A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6790



Internal ID15537073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:42907781..42929315hg38UCSC Ensembl
Outerchr19:43411933..43433467hg19UCSC Ensembl
Outerchr19:48103773..48125307hg18UCSC Ensembl
Outerchr19:48103773..48125307hg17UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3821535
hg1921535
hg1821535
hg1721535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2497
Supporting Variants
SamplesNA12156
Known GenesPSG6, PSG7
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)nssv6790
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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