A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947411



Internal ID18594259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:8300695..8313174hg38UCSC Ensembl
Innerchr1:8360755..8373234hg19UCSC Ensembl
Innerchr1:8283342..8295821hg18UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3812480
hg1912480
hg1812480
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2762787
SamplesHGDP00998
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947411
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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