A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3944355



Internal ID21364424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49549880..49549979hg38UCSC Ensembl
chr15:49842077..49842176hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15183248
SamplesHG002
Known GenesFAM227B
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3944355
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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