A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978908



Internal ID18267425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43356670..43377937hg38UCSC Ensembl
Innerchr19:43860822..43882089hg19UCSC Ensembl
Innerchr19:48552662..48573929hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3821268
hg1921268
hg1821268
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2761025
SamplesHGDP00778
Known GenesCD177
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv978908
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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