A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514628



Internal ID20887983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95929514..95936372hg38UCSC Ensembl
chr14:96395851..96402709hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg386859
hg196859
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022224
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514628
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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