A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2636



Internal ID15540475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:1265402..1284190hg38UCSC Ensembl
Outerchr7:1305038..1323826hg19UCSC Ensembl
Outerchr7:1271564..1290352hg18UCSC Ensembl
Outerchr7:1078279..1097067hg17UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg387208
hg197208
hg187208
hg177208
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5614
Supporting Variants
SamplesNA18555
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)nssv2636
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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