A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5531175



Internal ID307139
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 StatusM
Merged Variants
Supporting Variantsnssv17712647
Samples
Known GenesZNF207
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5531175
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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