A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336015



Internal ID20993568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38176451..38187982hg38UCSC Ensembl
chr2:38403593..38415124hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg3811532
hg1911532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089130
Samples
Known GenesCYP1B1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336015
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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