A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496881



Internal ID20870084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105864257..106652840hg38UCSC Ensembl
chr14:106330467..107108855hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38788584
hg19778389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2297n223
Supporting Variantsnssv18015894
Samples
Known GenesADAM6, KIAA0125, LINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496881
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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