A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496376



Internal ID20869577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99649424..99661182hg38UCSC Ensembl
chr15:100189629..100201387hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3811759
hg1911759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027984
Samples
Known GenesMEF2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496376
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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