A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528781



Internal ID304825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75786630..75787678hg38UCSC Ensembl
chr17:73782711..73783759hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381049
hg191049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714660
Samples
Known GenesUNK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528781
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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