A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604749



Internal ID20977820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:127394006..127401044hg38UCSC Ensembl
chr6:127715151..127722189hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg387039
hg197039
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215521
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604749
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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