A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571792



Internal ID20944863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35976147..35976753hg38UCSC Ensembl
chr6:35943924..35944530hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38607
hg19607
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270695
Samples
Known GenesSLC26A8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571792
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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