A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7937



Internal ID15535927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:22281372..22315531hg38UCSC Ensembl
Outerchr4:22282995..22317154hg19UCSC Ensembl
Outerchr4:21892093..21926252hg18UCSC Ensembl
Outerchr4:21959264..21993423hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg385280
hg195280
hg185280
hg175280
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4271
Supporting Variants
SamplesNA12156
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)nssv7937
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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