A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15706889



Internal ID21379165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:181908866..181909533hg38UCSC Ensembl
chr2:182773593..182774260hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg38668
hg19668
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4390088
Supporting Variants
Samples
Known GenesSSFA2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15706889
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0114943


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