A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5156



Internal ID15542920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:5218726..5260702hg38UCSC Ensembl
Outerchr10:5260689..5302665hg19UCSC Ensembl
Outerchr10:5250689..5292665hg18UCSC Ensembl
Outerchr10:5250689..5292665hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3841977
hg1941977
hg1841977
hg1741977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5643
Supporting Variants
SamplesNA19129
Known GenesAKR1C4
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)nssv5156
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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