A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7450



Internal ID15536414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:52077653..52122636hg38UCSC Ensembl
Outerchr19:52580906..52625889hg19UCSC Ensembl
Outerchr19:57272718..57317701hg18UCSC Ensembl
Outerchr19:57272718..57317701hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3844984
hg1944984
hg1844984
hg1744984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2535
Supporting Variants
SamplesNA12156
Known GenesZNF616, ZNF841
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)nssv7450
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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