A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10207



Internal ID15542591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:26323385..26330114hg38UCSC Ensembl
Outerchr2:26546253..26552982hg19UCSC Ensembl
Outerchr2:26399757..26406486hg18UCSC Ensembl
Outerchr2:26457904..26464633hg17UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg386413
hg196413
hg186413
hg176413
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2649
Supporting Variants
SamplesNA18956
Known GenesGPR113
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)nssv10207
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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