A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961301



Internal ID18249861
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 TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2759133
SamplesHGDP01029
Known GenesLOC100287534
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv961301
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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