A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587864



Internal ID20960935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:73620107..73620309hg38UCSC Ensembl
chr12:74013887..74014089hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233749
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587864
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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