A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3497



Internal ID15538225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:883838..901994hg38UCSC Ensembl
Outerchr7:923475..941631hg19UCSC Ensembl
Outerchr7:890001..908157hg18UCSC Ensembl
Outerchr7:696716..714872hg17UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg386301
hg196301
hg186301
hg176301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5611
Supporting Variants
SamplesNA12878
Known GenesADAP1, GET4
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)nssv3497
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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