A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037729



Internal ID20604769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76717946..76720017hg38UCSC Ensembl
chr17:74714028..74716099hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg382072
hg192072
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529318
Supporting Variants
Samples
Known GenesJMJD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037729
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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