A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510687



Internal ID20884008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90240665..90244608hg38UCSC Ensembl
chr15:90783897..90787840hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg383944
hg193944
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026941
Samples
Known GenesCIB1, GDPGP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510687
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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