A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4626



Internal ID15549354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:182757116..182767035hg38UCSC Ensembl
Outerchr4:183678269..183688188hg19UCSC Ensembl
Outerchr4:183915263..183925182hg18UCSC Ensembl
Outerchr4:184053418..184063337hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg389920
hg199920
hg189920
hg179920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8038
SamplesNA12156
Known GenesTENM3
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)nsv4626
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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