A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529368



Internal ID20902729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69104972..69106548hg38UCSC Ensembl
chr17:67101113..67102689hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg381577
hg191577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037593
Samples
Known GenesABCA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529368
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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