A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10409



Internal ID15542389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:74693630..74738953hg38UCSC Ensembl
Outerchr4:75618840..75664163hg19UCSC Ensembl
Outerchr4:75837864..75883187hg18UCSC Ensembl
Outerchr4:75976019..76021342hg17UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3845324
hg1945324
hg1845324
hg1745324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4390
Supporting Variants
SamplesNA18956
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)nssv10409
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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