A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1089394



Internal ID15595894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88039690..88041845hg38UCSC Ensembl
Innerchr7:87669005..87671160hg19UCSC Ensembl
Innerchr7:87506941..87509096hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg382156
hg192156
hg182156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607732
Supporting Variants
Samples
Known GenesADAM22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1089394
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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