A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1092078



Internal ID15945264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:106936413..106979027hg38UCSC Ensembl
Innerchr7:106576858..106619472hg19UCSC Ensembl
Innerchr7:106364094..106406708hg18UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3842615
hg1942615
hg1842615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608071
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1092078
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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