A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6775



Internal ID15537088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:19718214..19758362hg38UCSC Ensembl
Outerchr19:19829023..19869171hg19UCSC Ensembl
Outerchr19:19690023..19730171hg18UCSC Ensembl
Outerchr19:19690023..19730171hg17UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3840149
hg1940149
hg1840149
hg1740149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2436
Supporting Variants
SamplesNA12156
Known GenesLINC00663, ZNF14
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)nssv6775
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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