A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2581



Internal ID15193850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:32011510..32050248hg38UCSC Ensembl
Outerchr6:31979287..32018025hg19UCSC Ensembl
Outerchr6:32087265..32126003hg18UCSC Ensembl
Outerchr6:32087265..32126003hg17UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3838739
hg1938739
hg1838739
hg1738739
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5247
Supporting Variants
SamplesNA18555
Known GenesC4A, C4B, C4B_2, CYP21A2, STK19, TNXA, TNXB
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)nssv2581
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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