A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600675



Internal ID20973746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:3325922..3467294hg38UCSC Ensembl
chr7:3365554..3506926hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38141373
hg19141373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6541n223
Supporting Variantsnssv18156176
Samples
Known GenesSDK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600675
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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