A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003713



Internal ID18746244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:241832802..242092523hg38UCSC Ensembl
Innerchr2:242774979..243034674hg19UCSC Ensembl
Innerchr2:242423652..242683347hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38259722
hg19259696
hg18259696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4200n100
Supporting Variantsnssv3730134, nssv3587019
Samples
Known GenesCXXC11, LOC728323, PDCD1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003713
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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