A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10107



Internal ID15196004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:1717490..1749108hg38UCSC Ensembl
Outerchr17:1620784..1652402hg19UCSC Ensembl
Outerchr17:1567534..1599152hg18UCSC Ensembl
Outerchr17:1567534..1599152hg17UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg387887
hg197887
hg187887
hg177887
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1946
Supporting Variants
SamplesNA18956
Known GenesSERPINF2, WDR81
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)nssv10107
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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