A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3001699



Internal ID16947965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:26459433..26484332hg38UCSC Ensembl
Outerchr2:26682301..26707200hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3824900
hg1924900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953759
Supporting Variants
SamplesBILGI_BIOE
Known GenesOTOF
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3001699
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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