A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515128



Internal ID291613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75800971..75801575hg38UCSC Ensembl
chr17:73797052..73797656hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38605
hg19605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714662
Samples
Known GenesUNK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515128
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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