A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236581



Internal ID20803621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:51290379..51314407hg38UCSC Ensembl
chr7:51358076..51382104hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3824029
hg1924029
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608192
Supporting Variants
Samples
Known GenesCOBL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236581
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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