A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019359



Internal ID19108577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:57406148..57960277hg38UCSC Ensembl
Innerchr7:57473854..58019983hg19UCSC Ensembl
Innerchr7:57477796..58023925hg18UCSC Ensembl
Cytoband7p11.1
Allele length
AssemblyAllele length
hg38554130
hg19546130
hg18546130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6370n100
Supporting Variantsnssv3661493
Samples
Known GenesZNF716
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019359
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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