A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534000



Internal ID20907361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76454548..76454980hg38UCSC Ensembl
chr17:74450630..74451062hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38433
hg19433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038231
Samples
Known GenesAANAT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534000
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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