A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337305



Internal ID20994858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206235456..206243481hg38UCSC Ensembl
chr2:207100180..207108205hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg388026
hg198026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082950
Samples
Known GenesGPR1-AS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337305
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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