A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665



Internal ID15198514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:101003197..101022241hg38UCSC Ensembl
Outerchr7:100646478..100665522hg19UCSC Ensembl
Outerchr7:100433198..100452242hg18UCSC Ensembl
Outerchr7:100239913..100258957hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3821955
hg1921955
hg1821955
hg1721955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872
Supporting Variants
SamplesNA19240
Known GenesMUC12, MUC17
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)nssv665
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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