A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17715551



Internal ID139217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81046165..81046578hg38UCSC Ensembl
chr17:79019965..79020378hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5530722
Supporting Variants
Samples
Known GenesBAIAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17715551
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001093


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