A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262638



Internal ID20829678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27419290..27419594hg38UCSC Ensembl
chr3:27460781..27461085hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545240
Supporting Variants
Samples
Known GenesSLC4A7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262638
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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