A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503612



Internal ID20876868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39829078..39829479hg38UCSC Ensembl
chr15:40121279..40121680hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024190
Samples
Known GenesGPR176
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503612
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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