A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196975



Internal ID20764015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:61064944..61129461hg38UCSC Ensembl
chr17:59142305..59206822hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3864518
hg1964518
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522168
Supporting Variants
Samples
Known GenesBCAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196975
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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