A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17003185



Internal ID69737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129956928..129958051hg38UCSC Ensembl
chr7:129596768..129597891hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg381124
hg191124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480936
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17003185
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001093


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