A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16951478



Internal ID35007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82898047..82898105hg38UCSC Ensembl
chr4:83819200..83819258hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458375
Supporting Variants
Samples
Known GenesTHAP9-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16951478
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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