A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1622



Internal ID15546185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:77022478..77051924hg38UCSC Ensembl
Outerchr15:77314819..77344266hg19UCSC Ensembl
Outerchr15:75101874..75131321hg18UCSC Ensembl
Outerchr15:75101874..75131321hg17UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg387083
hg197083
hg187083
hg177083
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6643, nssv2118, nssv5568, nssv1266, nssv9960
SamplesNA18507, NA12156, NA18555, NA19240, NA19129
Known GenesPSTPIP1, TSPAN3
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)nsv1622
Frequency
Sample Size9
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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