A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18022247



Internal ID20589288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96471237..96474487hg38UCSC Ensembl
chr14:96937574..96940824hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg383251
hg193251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6506483
Supporting Variants
Samples
Known GenesAK7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18022247
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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