A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605765



Internal ID20978836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:52839219..52852849hg38UCSC Ensembl
chr7:52906912..52920542hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3813631
hg1913631
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230683
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605765
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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