A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316034



Internal ID20849110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:195638575..195672547hg38UCSC Ensembl
chr1:195607705..195641677hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3833973
hg1933973
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202004
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316034
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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