A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018761



Internal ID19107978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88507567..88626842hg38UCSC Ensembl
Innerchr7:88136882..88256156hg19UCSC Ensembl
Innerchr7:87974818..88094092hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38119276
hg19119275
hg18119275
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6524n100
Supporting Variantsnssv3655197
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018761
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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