A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3499953



Internal ID18740908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:180158481..180267317hg38UCSC Ensembl
Innerchr1:180127616..180236452hg19UCSC Ensembl
Innerchr1:178394239..178503075hg18UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38108837
hg19108837
hg18108837
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999182
Supporting Variants
Samples
Known GenesFLJ23867, LHX4, QSOX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3499953
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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