A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326345



Internal ID20859480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6727142..6733583hg38UCSC Ensembl
chr1:6787202..6793643hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg386442
hg196442
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204311
Samples
Known GenesLOC100505887
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326345
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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