A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499884



Internal ID20873109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78970488..78970937hg38UCSC Ensembl
chr15:79262830..79263279hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026788
Samples
Known GenesRASGRF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499884
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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