A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621187



Internal ID7008056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97244835..97245552hg38UCSC Ensembl
Innerchr9:97244838..97245549hg38UCSC Ensembl
Outerchr9:97244832..97245555hg38UCSC Ensembl
chr9:100007117..100007834hg19UCSC Ensembl
Innerchr9:100007120..100007831hg19UCSC Ensembl
Outerchr9:100007114..100007837hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38718
hg19718
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13573604, essv13573616, essv13573612, essv13573611, essv13573625, essv13573614, essv13573602, essv13573619, essv13573615, essv13573609, essv13573624, essv13573627, essv13573630, essv13573603, essv13573606, essv13573608, essv13573629, essv13573622, essv13573621, essv13573626, essv13573618, essv13573628, essv13573605, essv13573623, essv13573617, essv13573607, essv13573613, essv13573620, essv13573610
SamplesNA20882, NA20853, HG04229, HG04202, HG02734, HG03782, NA20900, HG03911, HG02597, HG04106, HG03744, NA21129, NA21114, HG00530, HG03697, NA20876, HG03951, HG03694, NA20851, HG04026, NA20902, NA21125, HG04015, NA20868, HG03977, NA21093, HG04056, HG03867, HG03864
Known GenesLOC100499484, LOC100499484-C9ORF174
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621187
Frequency
Sample Size2504
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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