A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9901



Internal ID15539982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:49662488..49702772hg38UCSC Ensembl
Outerchr7:49702084..49742368hg19UCSC Ensembl
Outerchr7:49672630..49712914hg18UCSC Ensembl
Outerchr7:49479345..49519629hg17UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg3840285
hg1940285
hg1840285
hg1740285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5736
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)nssv9901
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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