A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501547



Internal ID20874782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99959106..99961153hg38UCSC Ensembl
chr14:100425443..100427490hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg382048
hg192048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023161
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501547
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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