A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9888



Internal ID15539965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:26321365..26353863hg38UCSC Ensembl
Outerchr6:26321593..26354091hg19UCSC Ensembl
Outerchr6:26429572..26462070hg18UCSC Ensembl
Outerchr6:26429572..26462070hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3832499
hg1932499
hg1832499
hg1732499
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5230
Supporting Variants
SamplesNA18507
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)nssv9888
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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