A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6676



Internal ID15537187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:62573935..62619299hg38UCSC Ensembl
Outerchr16:62607839..62653203hg19UCSC Ensembl
Outerchr16:61165340..61210704hg18UCSC Ensembl
Outerchr16:61165340..61210704hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3845365
hg1945365
hg1845365
hg1745365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1827
Supporting Variants
SamplesNA12156
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)nssv6676
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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