A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3552399



Internal ID18503994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:51931192..52014941hg38UCSC Ensembl
Innerchr15:52223389..52307138hg19UCSC Ensembl
Innerchr15:50010681..50094430hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3883750
hg1983750
hg1883750
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053788
Supporting Variants
Samples
Known GenesLEO1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3552399
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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