A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017577



Internal ID18760111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12490865..12683322hg38UCSC Ensembl
Innerchr7:12530491..12722947hg19UCSC Ensembl
Innerchr7:12497016..12689472hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38192458
hg19192457
hg18192457
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6274n100
Supporting Variantsnssv3642978
Samples
Known GenesSCIN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017577
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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