A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608686



Internal ID20981757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:63836539..64068427hg38UCSC Ensembl
chr7:63296917..63528805hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38231889
hg19231889
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233947
Samples
Known GenesLINC01005, ZNF727
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608686
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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