A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16996201



Internal ID64917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38071929..38073642hg38UCSC Ensembl
chr7:38111531..38113244hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg381714
hg191714
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5564045
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16996201
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.068061


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