A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609573



Internal ID20982644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12034953..12060590hg38UCSC Ensembl
chr7:12074579..12100216hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3825638
hg1925638
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223397
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609573
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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