A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600449



Internal ID20973520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:148045939..148069242hg38UCSC Ensembl
chr6:148367075..148390378hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3823304
hg1923304
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217070
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600449
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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