A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9873



Internal ID15539948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:3522384..3563974hg38UCSC Ensembl
Outerchr3:3564068..3605658hg19UCSC Ensembl
Outerchr3:3539068..3580658hg18UCSC Ensembl
Outerchr3:3539068..3580658hg17UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3841591
hg1941591
hg1841591
hg1741591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3678
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)nssv9873
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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