A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3664287



Internal ID18615882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:141537133..141590700hg38UCSC Ensembl
Innerchr7:141236933..141290500hg19UCSC Ensembl
Innerchr7:140883402..140936969hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3853568
hg1953568
hg1853568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034207
Supporting Variants
Samples
Known GenesAGK
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3664287
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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