A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv708766



Internal ID15656036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:3009815..3089567hg38UCSC Ensembl
Innerchr1:2926379..3006131hg19UCSC Ensembl
Innerchr1:2916239..2995991hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3879753
hg1979753
hg1879753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545098
Supporting Variants
Samples
Known GenesACTRT2, LINC00982, PRDM16
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv708766
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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