A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16916078



Internal ID11436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:71294428..71344645hg38UCSC Ensembl
chr2:71521558..71571775hg19UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg3850218
hg1950218
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562350
Supporting Variants
Samples
Known GenesZNF638
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16916078
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.001093


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