A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189574



Internal ID20756614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74696613..74700527hg38UCSC Ensembl
chr10:76456371..76460285hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg383915
hg193915
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453172
Supporting Variants
Samples
Known GenesADK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189574
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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