A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673



Internal ID15545247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:106318714..106339608hg38UCSC Ensembl
Outerchr7:105959160..105980054hg19UCSC Ensembl
Outerchr7:105746396..105767290hg18UCSC Ensembl
Outerchr7:105553111..105574005hg17UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg387891
hg197891
hg187891
hg177891
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5892
Supporting Variants
SamplesNA19240
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)nssv673
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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