A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17001022



Internal ID68255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74858779..74876779hg38UCSC Ensembl
chr7:74275074..74292873hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3818001
hg1917800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488654
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17001022
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000314


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