A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613772



Internal ID20986843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:3152540..3227716hg38UCSC Ensembl
chr7:3192173..3267348hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3875177
hg1975176
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231778
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613772
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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