A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525534



Internal ID20898895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:55702155..55702862hg38UCSC Ensembl
chr17:53779516..53780223hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38708
hg19708
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036946
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525534
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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