A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482152



Internal ID21139705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77745317..77750051hg38UCSC Ensembl
chr14:78211660..78216394hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg384735
hg194735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020870
Samples
Known GenesSNW1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482152
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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