A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496739



Internal ID20869942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:12817061..12817488hg38UCSC Ensembl
chr17:12720378..12720805hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38428
hg19428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034215
Samples
Known GenesARHGAP44
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496739
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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