A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612084



Internal ID20985155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:3183400..3428630hg38UCSC Ensembl
chr7:3223032..3468262hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38245231
hg19245231
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224085
Samples
Known GenesSDK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612084
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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