A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16985388



Internal ID57665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89879350..89910750hg38UCSC Ensembl
chr6:90589069..90620469hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3831401
hg1931401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5468890
Supporting Variants
Samples
Known GenesGJA10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16985388
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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