A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347627



Internal ID21005180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:201887573..201888264hg38UCSC Ensembl
chr2:202752296..202752987hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38692
hg19692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084609
Samples
Known GenesCDK15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347627
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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