A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605862



Internal ID16046585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2516523..2604885hg38UCSC Ensembl
Innerchr7:2556157..2644519hg19UCSC Ensembl
Innerchr7:2522683..2611045hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3888363
hg1988363
hg1888363
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1078470
Samples
Known GenesBRAT1, IQCE, LFNG, MIR4648
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605862
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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