A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533402



Internal ID20906763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81040995..81046530hg38UCSC Ensembl
chr17:79014795..79020330hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg385536
hg195536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038522
Samples
Known GenesBAIAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533402
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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