A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602929



Internal ID20976000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:467207..467825hg38UCSC Ensembl
chr7:506844..507462hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38619
hg19619
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222730
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602929
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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