A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16995522



Internal ID64456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44844613..44846503hg38UCSC Ensembl
chr7:44884212..44886102hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg381891
hg191891
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557040
Supporting Variants
Samples
Known GenesH2AFV
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16995522
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.001093


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