A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499390



Internal ID20872609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64363206..64365253hg38UCSC Ensembl
chr15:64655405..64657452hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg382048
hg192048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025664
Samples
Known GenesKIAA0101
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499390
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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