A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8647



Internal ID15535217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:100728545..100773371hg38UCSC Ensembl
Outerchr9:103490827..103535653hg19UCSC Ensembl
Outerchr9:102530648..102575474hg18UCSC Ensembl
Outerchr9:100570382..100615208hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3844827
hg1944827
hg1844827
hg1744827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6640
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)nssv8647
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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