A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478137



Internal ID21135690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:72703259..72707320hg38UCSC Ensembl
chr14:73169967..73174028hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg384062
hg194062
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021059
Samples
Known GenesDPF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478137
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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