A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010656



Internal ID18753188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:241830506..242084095hg38UCSC Ensembl
Innerchr2:242772683..243026246hg19UCSC Ensembl
Innerchr2:242421356..242674919hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38253590
hg19253564
hg18253564
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4200n100
Supporting Variantsnssv3587014, nssv3587016, nssv3587011, nssv3730132, nssv3587012, nssv3587013, nssv3587015
Samples
Known GenesCXXC11, PDCD1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010656
Frequency
Sample Size29084
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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