A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17005667



Internal ID71391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149027645..149027726hg38UCSC Ensembl
chr7:148724737..148724818hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476901
Supporting Variants
Samples
Known GenesPDIA4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17005667
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.012804


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