A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514590



Internal ID20887945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95279292..95290042hg38UCSC Ensembl
chr14:95745629..95756379hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3810751
hg1910751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022200
Samples
Known GenesCLMN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514590
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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