A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1608



Internal ID15546171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:74265520..74297620hg38UCSC Ensembl
Outerchr15:74557861..74589961hg19UCSC Ensembl
Outerchr15:72344914..72377014hg18UCSC Ensembl
Outerchr15:72344914..72377014hg17UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg387335
hg197335
hg187335
hg177335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6641
SamplesNA12156
Known GenesCCDC33
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)nsv1608
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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