A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16924690



Internal ID17206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:203948268..203948291hg38UCSC Ensembl
chr2:204812991..204813014hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg3824
hg1924
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555448
Supporting Variants
Samples
Known GenesICOS
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16924690
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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