A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3003390



Internal ID17296342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:23743028..23745714hg38UCSC Ensembl
Outerchr6:23743256..23745942hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382687
hg192687
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv955816
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3003390
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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