A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506639



Internal ID20879922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41397565..41408005hg38UCSC Ensembl
chr15:41689763..41700203hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3810441
hg1910441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023881
Samples
Known GenesNDUFAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506639
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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