A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508567



Internal ID20881870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90580705..90584082hg38UCSC Ensembl
chr15:91123937..91127314hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg383378
hg193378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027375
Samples
Known GenesCRTC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508567
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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