A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3515053



Internal ID18466648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:88740764..88766622hg38UCSC Ensembl
Innerchr10:90500521..90526379hg19UCSC Ensembl
Innerchr10:90490501..90516359hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3825859
hg1925859
hg1825859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052613
Supporting Variants
Samples
Known GenesLIPK, LIPN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3515053
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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