A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525332



Internal ID20898693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68255876..68256813hg38UCSC Ensembl
chr17:66252017..66252954hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38938
hg19938
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037480
Samples
Known GenesAMZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525332
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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