A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496997



Internal ID20870200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52162015..52163490hg38UCSC Ensembl
chr15:52454212..52455687hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg381476
hg191476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024056
Samples
Known GenesGNB5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496997
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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