A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425877



Internal ID21083430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:136094401..136107600hg38UCSC Ensembl
chr7:135779149..135792348hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3813200
hg1913200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225772
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425877
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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