A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1624



Internal ID15546187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:77515279..77552477hg38UCSC Ensembl
Outerchr15:77807621..77844819hg19UCSC Ensembl
Outerchr15:75594676..75631874hg18UCSC Ensembl
Outerchr15:75594676..75631874hg17UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg385268
hg195268
hg185268
hg175268
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10065, nssv7203
SamplesNA12156, NA18956
Known Genes
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)nsv1624
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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