A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3943427



Internal ID21363496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56109469..56109858hg38UCSC Ensembl
chr15:56401667..56402056hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15183270
SamplesHG002
Known GenesRFX7
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3943427
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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