A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150428



Internal ID15529338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:44931099..44967150hg38UCSC Ensembl
Innerchr2:45158238..45194289hg19UCSC Ensembl
Innerchr2:45011742..45047793hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3836052
hg1936052
hg1836052
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581702
Supporting Variants
SamplesHGDP00774
Known GenesSIX3, SIX3-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150428
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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