A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145296



Internal ID344501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5868421..5886961hg38UCSC Ensembl
chr17:5771741..5790281hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3818541
hg1918541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17711083
Samples
Known GenesLOC339166
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145296
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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