A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339101



Internal ID20996654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:37203862..37205678hg38UCSC Ensembl
chr2:37431005..37432821hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg381817
hg191817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089090
Samples
Known GenesCEBPZ, CEBPZ-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339101
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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