A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8604



Internal ID15535260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:36660250..36704974hg38UCSC Ensembl
Outerchr9:36660247..36704971hg19UCSC Ensembl
Outerchr9:36650247..36694971hg18UCSC Ensembl
Outerchr9:36650247..36694971hg17UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3844725
hg1944725
hg1844725
hg1744725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530
Supporting Variants
SamplesNA12156
Known GenesMELK
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)nssv8604
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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