A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3514697



Internal ID18466292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:88707310..88833935hg38UCSC Ensembl
Innerchr10:90467067..90593692hg19UCSC Ensembl
Innerchr10:90457047..90583672hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38126626
hg19126626
hg18126626
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043015
Supporting Variants
Samples
Known GenesANKRD22, LIPK, LIPM, LIPN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3514697
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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