A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7938



Internal ID15535926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:24173897..24183665hg38UCSC Ensembl
Outerchr4:24175520..24185288hg19UCSC Ensembl
Outerchr4:23784618..23794386hg18UCSC Ensembl
Outerchr4:23851789..23861557hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg389769
hg199769
hg189769
hg179769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4275
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)nssv7938
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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