A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17006371



Internal ID71872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142619746..142620359hg38UCSC Ensembl
chr7:142327260..142327873hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38614
hg19614
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476791
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17006371
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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