A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203098



Internal ID20770138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40467176..40497957hg38UCSC Ensembl
chr1:40932848..40963629hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3830782
hg1930782
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6315914
Supporting Variants
Samples
Known GenesZFP69
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203098
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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