A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258983



Internal ID20826023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:72767834..72768622hg38UCSC Ensembl
chr2:72994963..72995751hg19UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg38789
hg19789
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545235
Supporting Variants
Samples
Known GenesEXOC6B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258983
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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