A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18156520



Internal ID20723560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:3843786..3868309hg38UCSC Ensembl
chr7:3883418..3907941hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3824524
hg1924524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617647
Supporting Variants
Samples
Known GenesSDK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18156520
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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