A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524689



Internal ID20898050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78274825..78282911hg38UCSC Ensembl
chr17:76270906..76278992hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg388087
hg198087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038094
Samples
Known GenesLOC100996291
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524689
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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