A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1260



Internal ID15544465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:70713112..70736445hg38UCSC Ensembl
Outerchr15:71005451..71028784hg19UCSC Ensembl
Outerchr15:68792505..68815838hg18UCSC Ensembl
Outerchr15:68792505..68815838hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3823334
hg1923334
hg1823334
hg1723334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1595
Supporting Variants
SamplesNA19240
Known GenesUACA
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)nssv1260
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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