A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498158



Internal ID20871366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42550721..42558599hg38UCSC Ensembl
chr15:42842919..42850797hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg387879
hg197879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2506n223
Supporting Variantsnssv18023944
Samples
Known GenesHAUS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498158
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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