A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505821



Internal ID20879094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:12016438..12018994hg38UCSC Ensembl
chr17:11919755..11922311hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg382557
hg192557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034145
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505821
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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