A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505925



Internal ID20879199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93027921..93046540hg38UCSC Ensembl
chr15:93571151..93589770hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3818620
hg1918620
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182654
Samples
Known GenesCHD2, RGMA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505925
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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