A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530066



Internal ID20903427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77619727..77638898hg38UCSC Ensembl
chr17:75615809..75634980hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3819172
hg1919172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039025
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530066
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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