A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022156



Internal ID19111374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:97743111..97772903hg38UCSC Ensembl
Innerchr7:97372423..97402215hg19UCSC Ensembl
Innerchr7:97210359..97240151hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3829793
hg1929793
hg1829793
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6534n100
Supporting Variantsnssv3655254
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)nsv1022156
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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