A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607752



Internal ID20980823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122195500..122289880hg38UCSC Ensembl
chr7:121835554..121929934hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3894381
hg1994381
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234723
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607752
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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