A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10981



Internal ID15539569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:112147480..112168678hg38UCSC Ensembl
Outerchr1:112690102..112711300hg19UCSC Ensembl
Outerchr1:112491625..112512823hg18UCSC Ensembl
Outerchr1:112402144..112423342hg17UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3821199
hg1921199
hg1821199
hg1721199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2443
Supporting Variants
SamplesNA15510
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)nssv10981
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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