A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1089430



Internal ID15595930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88040094..88042153hg38UCSC Ensembl
Innerchr7:87669409..87671468hg19UCSC Ensembl
Innerchr7:87507345..87509404hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg382060
hg192060
hg182060
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607738
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)nssv1089430
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer