A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5952



Internal ID15550813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:131764570..131796156hg38UCSC Ensembl
Outerchr7:131449329..131480915hg19UCSC Ensembl
Outerchr7:131099869..131131455hg18UCSC Ensembl
Outerchr7:130906584..130938170hg17UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg388160
hg198160
hg188160
hg178160
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3579
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)nsv5952
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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