A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1543



Internal ID15546106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:55934091..55986219hg38UCSC Ensembl
Outerchr15:56226289..56278417hg19UCSC Ensembl
Outerchr15:54013581..54065709hg18UCSC Ensembl
Outerchr15:54013581..54065709hg17UCSC 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 StatusM
Merged Variants
Supporting Variantsnssv10055, nssv1253, nssv7174, nssv2936
SamplesNA12156, NA18956, NA18555, NA19240
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)nsv1543
Frequency
Sample Size9
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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