A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530293



Internal ID20903654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:66989013..66989954hg38UCSC Ensembl
chr17:64985129..64986070hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38942
hg19942
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037375
Samples
Known GenesCACNG4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530293
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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