A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652



Internal ID15550483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:20787999..20821498hg38UCSC Ensembl
Outerchr7:20827618..20861117hg19UCSC Ensembl
Outerchr7:20794143..20827642hg18UCSC Ensembl
Outerchr7:20600858..20634357hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg385765
hg195765
hg185765
hg175765
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4971
SamplesNA19129
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)nsv5652
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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