A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2675



Internal ID15540432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:98755405..98791288hg38UCSC Ensembl
Outerchr7:98384738..98388911hg19UCSC Ensembl
Outerchr7:98222674..98226847hg18UCSC Ensembl
Outerchr7:98029389..98033562hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3831671
hg1931671
hg1831671
hg1731671
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5862
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)nssv2675
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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