A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540957



Internal ID20914244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27670254..27670808hg38UCSC Ensembl
chr2:27893121..27893675hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38555
hg19555
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257559
Samples
Known GenesSLC4A1AP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540957
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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