A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326777



Internal ID20859914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:4078027..4135145hg38UCSC Ensembl
chr1:4138087..4195205hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3857119
hg1957119
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203104
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326777
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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