A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602719



Internal ID20975790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:124170526..124280396hg38UCSC Ensembl
chr7:123810580..123920450hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg38109871
hg19109871
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235945
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602719
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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