A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523546



Internal ID20896907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76715599..76716035hg38UCSC Ensembl
chr17:74711681..74712117hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037730
Samples
Known GenesJMJD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523546
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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