A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524148



Internal ID20897509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69099488..69100267hg38UCSC Ensembl
chr17:67095629..67096408hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38780
hg19780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037591
Samples
Known GenesABCA6, MIR4524A, MIR4524B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524148
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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