A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016762



Internal ID19105979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111129012..111243423hg38UCSC Ensembl
Innerchr7:110769068..110883479hg19UCSC Ensembl
Innerchr7:110556304..110670715hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38114412
hg19114412
hg18114412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6565n100
Supporting Variantsnssv3645221
Samples
Known GenesIMMP2L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016762
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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