A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495693



Internal ID20868887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99568366..99569016hg38UCSC Ensembl
chr15:100108571..100109221hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38651
hg19651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027757
Samples
Known GenesMEF2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495693
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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