A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150785



Internal ID15875904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88318068..88545622hg38UCSC Ensembl
Innerchr2:88617587..88845140hg19UCSC Ensembl
Innerchr2:88398702..88626255hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38227555
hg19227554
hg18227554
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582387
Supporting Variants
SamplesHGDP00753
Known GenesFOXI3, TEX37
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150785
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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