A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606410



Internal ID16047133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:23293751..23343516hg38UCSC Ensembl
Innerchr7:23333370..23383135hg19UCSC Ensembl
Innerchr7:23299895..23349660hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3849766
hg1949766
hg1849766
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155845
Samples1780854545_A
Known GenesIGF2BP3, MALSU1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606410
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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