A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6844



Internal ID15537019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:65949791..65981525hg38UCSC Ensembl
Outerchr2:66176925..66208659hg19UCSC Ensembl
Outerchr2:66030429..66062163hg18UCSC Ensembl
Outerchr2:66088576..66120310hg17UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3831735
hg1931735
hg1831735
hg1731735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2760
Supporting Variants
SamplesNA12156
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv6844
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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