A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13433560



Internal ID2719111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26648109..26699631hg38UCSC Ensembl
Innerchr9:26648109..26699631hg38UCSC Ensembl
Outerchr9:26647609..26700131hg38UCSC Ensembl
chr9:26648107..26699629hg19UCSC Ensembl
Innerchr9:26648107..26699629hg19UCSC Ensembl
Outerchr9:26647607..26700129hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3851523
hg1951523
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620111
Supporting Variants
SamplesHG02396
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13433560
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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