A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504325



Internal ID20877586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37066805..37067118hg38UCSC Ensembl
chr15:37359006..37359319hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024371
Samples
Known GenesMEIS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504325
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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