A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17006203



Internal ID71764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135678143..135679900hg38UCSC Ensembl
chr7:135362891..135364648hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381758
hg191758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476093
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17006203
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002029


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