A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704992



Internal ID21377268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:127182766..127182847hg38UCSC Ensembl
chr10:128981030..128981111hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4389601
Supporting Variants
Samples
Known GenesDOCK1, FAM196A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704992
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00574713


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