A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543348



Internal ID20916597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68154529..68155506hg38UCSC Ensembl
chr2:68381661..68382638hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38978
hg19978
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3915n223
Supporting Variantsnssv18258831
Samples
Known GenesWDR92
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543348
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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