A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509749



Internal ID20883060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60023901..60058762hg38UCSC Ensembl
chr15:60316100..60350961hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3834862
hg1934862
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026015
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509749
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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