A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv971660



Internal ID16265616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119028154..119098548hg38UCSC Ensembl
Innerchr3:118747001..118817395hg19UCSC Ensembl
Innerchr3:120229691..120300085hg18UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg3870395
hg1970395
hg1870395
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591360
Supporting Variants
Samples
Known GenesIGSF11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv971660
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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