A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1638



Internal ID15546201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:81509540..81548134hg38UCSC Ensembl
Outerchr15:81801881..81840475hg19UCSC Ensembl
Outerchr15:79588936..79627530hg18UCSC Ensembl
Outerchr15:79588936..79627530hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3838595
hg1938595
hg1838595
hg1738595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7207
SamplesNA12156
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)nsv1638
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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