A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15183248



Internal ID21322044
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3944355
Supporting Variants
SamplesHG002
Known GenesFAM227B
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15183248
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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