A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514781



Internal ID20888136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26071302..26071740hg38UCSC Ensembl
chr15:26316449..26316887hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38439
hg19439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023252
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514781
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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