A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498108



Internal ID20871316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80076397..80076830hg38UCSC Ensembl
chr15:80368739..80369172hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026849
Samples
Known GenesZFAND6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498108
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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