A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4600



Internal ID15539327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:20707404..20714858hg38UCSC Ensembl
Outerchr3:20748896..20756350hg19UCSC Ensembl
Outerchr3:20723900..20731354hg18UCSC Ensembl
Outerchr3:20723900..20731354hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg385878
hg195878
hg185878
hg175878
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3726
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)nssv4600
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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