A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497886



Internal ID20871094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:94319489..94960830hg38UCSC Ensembl
chr15:94862718..95504059hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38641342
hg19641342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027047
Samples
Known GenesLOC440311, MCTP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497886
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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