A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502700



Internal ID20875947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101245268..101404689hg38UCSC Ensembl
chr14:101711605..101871026hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38159422
hg19159422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016501
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502700
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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