A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037742



Internal ID20604782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63957876..63986846hg38UCSC Ensembl
chr17:62035236..62064206hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg3828971
hg1928971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527951
Supporting Variants
Samples
Known GenesSCN4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037742
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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