A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508437



Internal ID20881737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55345166..55351350hg38UCSC Ensembl
chr15:55637364..55643548hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg386185
hg196185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024833
Samples
Known GenesPIGB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508437
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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