A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537703



Internal ID20911038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:46610548..46611429hg38UCSC Ensembl
chr2:46837687..46838568hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38882
hg19882
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258020
Samples
Known GenesPIGF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537703
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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