A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1625



Internal ID15546188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:77735492..77768973hg38UCSC Ensembl
Outerchr15:78027834..78061315hg19UCSC Ensembl
Outerchr15:75814889..75848370hg18UCSC Ensembl
Outerchr15:75814889..75848370hg17UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg385780
hg195780
hg185780
hg175780
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5569
SamplesNA19129
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)nsv1625
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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