A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943864



Internal ID22719320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37066805..37067117hg38UCSC Ensembl
chr15:37359006..37359318hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383027
Samples
Known GenesMEIS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943864
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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