A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516596



Internal ID20889957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71910045..71933421hg38UCSC Ensembl
chr17:69906186..69929562hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3823377
hg1923377
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192425
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516596
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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