A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150741



Internal ID15507872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:158795222..159096954hg38UCSC Ensembl
Innerchr2:159651734..159953466hg19UCSC Ensembl
Innerchr2:159359980..159661712hg18UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38301733
hg19301733
hg18301733
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583449
Supporting Variants
Samples1780862197_A
Known GenesDAPL1, TANC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150741
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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