A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145839



Internal ID345044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60550986..60551296hg38UCSC Ensembl
chr17:58628347..58628657hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17724898
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145839
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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