A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052613



Internal ID18795144
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 StatusM
Merged Variants
Supporting Variantsnssv3515053
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)nsv1052613
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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