A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3730131



Internal ID18681726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:241786337..242092523hg38UCSC Ensembl
Innerchr2:242725752..243034674hg19UCSC Ensembl
Innerchr2:242374425..242683347hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38306187
hg19308923
hg18308923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011971
Supporting Variants
Samples
Known GenesCXXC11, GAL3ST2, LOC728323, NEU4, PDCD1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3730131
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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