A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16925320



Internal ID17626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:142278771..142279337hg38UCSC Ensembl
chr2:143036340..143036906hg19UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562158
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16925320
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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