A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999232



Internal ID19158768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15805324..15823408hg38UCSC Ensembl
Innerchr1:16131819..16149903hg19UCSC Ensembl
Innerchr1:16004406..16022490hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3818085
hg1918085
hg1818085
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv36n100
Supporting Variantsnssv3698787
Samples
Known GenesUQCRHL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999232
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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