A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316636



Internal ID20849716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38868672..38870560hg38UCSC Ensembl
chr1:39334344..39336232hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381889
hg191889
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203063
Samples
Known GenesGJA9-MYCBP, MYCBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316636
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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