A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257773



Internal ID20824813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202897662..202898157hg38UCSC Ensembl
chr2:203762385..203762880hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542155
Supporting Variants
Samples
Known GenesWDR12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257773
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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