A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6634



Internal ID15190544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:56487384..56533662hg38UCSC Ensembl
Outerchr15:56779582..56825860hg19UCSC Ensembl
Outerchr15:54566874..54613152hg18UCSC Ensembl
Outerchr15:54566874..54613152hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3846279
hg1946279
hg1846279
hg1746279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1545
Supporting Variants
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)nssv6634
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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