A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2759133



Internal ID17512096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54790944..54798475hg38UCSC Ensembl
Innerchr19:55302396..55309930hg19UCSC Ensembl
Innerchr19:59994208..60001742hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg387532
hg197535
hg187535
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv961301
Supporting Variants
SamplesHGDP01029
Known GenesLOC100287534
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2759133
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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