A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508983



Internal ID20882288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42552312..42558570hg38UCSC Ensembl
chr15:42844510..42850768hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg386259
hg196259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2506n223
Supporting Variantsnssv18023946
Samples
Known GenesHAUS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508983
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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