A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219609



Internal ID20786649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23595601..23601600hg38UCSC Ensembl
chr7:23635220..23641219hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617878
Supporting Variants
Samples
Known GenesCCDC126
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219609
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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