A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18020372



Internal ID20587412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61767779..61774987hg38UCSC Ensembl
chr14:62234497..62241705hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg387209
hg197209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6489176
Supporting Variants
Samples
Known GenesSNAPC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18020372
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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