A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207438



Internal ID20774479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:175092101..175133400hg38UCSC Ensembl
chr2:175956829..175998128hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3841300
hg1941300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6341654
Supporting Variants
Samples
Known GenesATF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207438
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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