A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513233



Internal ID20886574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5965564..5966167hg38UCSC Ensembl
chr17:5868884..5869487hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38604
hg19604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036382
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513233
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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