A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513991



Internal ID20887340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38488801..38489700hg38UCSC Ensembl
chr15:38781002..38781901hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024106
Samples
Known GenesRASGRP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513991
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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