A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18038081



Internal ID20605121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78159569..78161746hg38UCSC Ensembl
chr17:76155650..76157827hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg382178
hg192178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523560
Supporting Variants
Samples
Known GenesC17orf99
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18038081
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00025


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