A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1083566



Internal ID15936752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:44960264..44961619hg38UCSC Ensembl
Innerchr7:44999863..45001218hg19UCSC Ensembl
Innerchr7:44966388..44967743hg18UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg381356
hg191356
hg181356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606815
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)nssv1083566
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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