A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333029



Internal ID20866204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6242901..6249500hg38UCSC Ensembl
chr1:6302961..6309560hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg386600
hg196600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203661
Samples
Known GenesGPR153, HES3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333029
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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