A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16997810



Internal ID66078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74934779..74955000hg38UCSC Ensembl
chr7:74349765..74369889hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3820222
hg1920125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474837
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16997810
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001103


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