A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9909



Internal ID15539991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:93769752..93804521hg38UCSC Ensembl
Outerchr7:93399064..93433833hg19UCSC Ensembl
Outerchr7:93237000..93271769hg18UCSC Ensembl
Outerchr7:93043715..93078484hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3834770
hg1934770
hg1834770
hg1734770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848
Supporting Variants
SamplesNA18507
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)nssv9909
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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