A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4618



Internal ID15196664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:130877388..130921852hg38UCSC Ensembl
Outerchr9:133752775..133797239hg19UCSC Ensembl
Outerchr9:132742596..132787060hg18UCSC Ensembl
Outerchr9:130782329..130826793hg17UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg3844465
hg1944465
hg1844465
hg1744465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6735
Supporting Variants
SamplesNA19129
Known GenesABL1, FIBCD1, QRFP
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)nssv4618
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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