A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016617



Internal ID19105834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:122130387..122180676hg38UCSC Ensembl
Innerchr7:121770441..121820730hg19UCSC Ensembl
Innerchr7:121557677..121607966hg18UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3850290
hg1950290
hg1850290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3662118, nssv3662117
Samples
Known GenesAASS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016617
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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