A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190650



Internal ID20757690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100245216..100253766hg38UCSC Ensembl
chr14:100711553..100720103hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg388551
hg198551
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499996
Supporting Variants
Samples
Known GenesYY1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190650
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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