A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1565



Internal ID15546128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:63686766..63704414hg38UCSC Ensembl
Outerchr15:63978965..63996613hg19UCSC Ensembl
Outerchr15:61766018..61783666hg18UCSC Ensembl
Outerchr15:61766018..61783666hg17UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3817649
hg1917649
hg1817649
hg1717649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7184
SamplesNA12156
Known GenesHERC1
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)nsv1565
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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