A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531679



Internal ID20905040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77266301..77277200hg38UCSC Ensembl
chr17:75262383..75273282hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3810900
hg1910900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3251n223
Supporting Variantsnssv18038992
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531679
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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