A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585165



Internal ID6625483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9111782..9116226hg38UCSC Ensembl
Innerchr1:9111843..9116165hg38UCSC Ensembl
Outerchr1:9111721..9116287hg38UCSC Ensembl
chr1:9171841..9176285hg19UCSC Ensembl
Innerchr1:9171902..9176224hg19UCSC Ensembl
Outerchr1:9171780..9176346hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg384445
hg194445
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9850193, essv9850192, essv9850194
SamplesHG04238, NA18983, HG03772
Known GenesGPR157
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585165
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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