A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609693



Internal ID20982764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:4055927..4133517hg38UCSC Ensembl
chr7:4095559..4173149hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3877591
hg1977591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153804
Samples
Known GenesSDK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609693
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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