A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575695



Internal ID20948766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6293433..6293950hg38UCSC Ensembl
chr12:6402599..6403116hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38518
hg19518
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225042
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575695
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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