A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8175



Internal ID15189003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:157454904..157490416hg38UCSC Ensembl
Outerchr5:156881912..156917424hg19UCSC Ensembl
Outerchr5:156814490..156850002hg18UCSC Ensembl
Outerchr5:156814490..156850002hg17UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3835513
hg1935513
hg1835513
hg1735513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5089
Supporting Variants
SamplesNA12156
Known GenesADAM19, NIPAL4
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)nssv8175
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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