A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17004441



Internal ID70598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141578102..141584072hg38UCSC Ensembl
chr7:141277902..141283872hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg385971
hg195971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476000
Supporting Variants
Samples
Known GenesAGK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17004441
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.007027


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