A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190877



Internal ID20757917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62806861..62819915hg38UCSC Ensembl
chr17:60884222..60897276hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3813055
hg1913055
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531102
Supporting Variants
Samples
Known GenesMARCH10, MIR548W
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190877
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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