A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523



Internal ID15538251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:42481294..42508875hg38UCSC Ensembl
Outerchr7:42520893..42548474hg19UCSC Ensembl
Outerchr7:42487418..42514999hg18UCSC Ensembl
Outerchr7:42294133..42321714hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg384882
hg194882
hg184882
hg174882
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5718
Supporting Variants
SamplesNA12878
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)nssv3523
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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