A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515736



Internal ID20889097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75424657..75451220hg38UCSC Ensembl
chr17:73420738..73447301hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3826564
hg1926564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037528
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515736
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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