A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550344



Internal ID20923492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6693883..6695574hg38UCSC Ensembl
chr1:6753943..6755634hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg381692
hg191692
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251254
Samples
Known GenesDNAJC11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550344
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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