A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977999



Internal ID52737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3183019..3185199hg38UCSC Ensembl
chr6:3183253..3185433hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg382181
hg192181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5468436
Supporting Variants
Samples
Known GenesLOC100507194
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977999
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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