A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712647



Internal ID136313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32352264..32354865hg38UCSC Ensembl
chr17:30679283..30681884hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg382602
hg192602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531175
Supporting Variants
Samples
Known GenesZNF207
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712647
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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