A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258952



Internal ID20825992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:70984841..71331694hg38UCSC Ensembl
chr2:71211971..71558824hg19UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg38346854
hg19346854
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540618
Supporting Variants
Samples
Known GenesANKRD53, MCEE, MPHOSPH10, NAGK, OR7E91P, PAIP2B, TEX261
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258952
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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