A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527639



Internal ID20901000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77579025..77587722hg38UCSC Ensembl
chr17:75575107..75583804hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg388698
hg198698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039019
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527639
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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