A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16997815



Internal ID66083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74968779..74978000hg38UCSC Ensembl
chr7:74382929..74392141hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg389222
hg199213
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142620
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16997815
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.013388


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