A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7174



Internal ID15536690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:55934091..55967111hg38UCSC Ensembl
Outerchr15:56226289..56259309hg19UCSC Ensembl
Outerchr15:54013581..54046601hg18UCSC Ensembl
Outerchr15:54013581..54046601hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg386416
hg196416
hg186416
hg176416
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1543
Supporting Variants
SamplesNA12156
Known GenesNEDD4
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)nssv7174
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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