A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3725



Internal ID15538453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:70699338..70748182hg38UCSC Ensembl
Outerchr9:73314254..73363098hg19UCSC Ensembl
Outerchr9:72504074..72552918hg18UCSC Ensembl
Outerchr9:70543808..70592652hg17UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3848845
hg1948845
hg1848845
hg1748845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556
Supporting Variants
SamplesNA12878
Known GenesTRPM3
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)nssv3725
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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