A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037194



Internal ID20604234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62760911..62761348hg38UCSC Ensembl
chr17:60838272..60838709hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38438
hg19438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519856
Supporting Variants
Samples
Known GenesMARCH10, MIR548W
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037194
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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