A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204355



Internal ID20771395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:71111611..71124230hg38UCSC Ensembl
chr1:71577294..71589913hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3812620
hg1912620
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6326445
Supporting Variants
Samples
Known GenesZRANB2-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204355
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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