A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476990



Internal ID21134543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51355891..51358185hg38UCSC Ensembl
chr14:51822609..51824903hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg382295
hg192295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019139
Samples
Known GenesLINC00640
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476990
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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