A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575819



Internal ID20948890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73178267..73179308hg38UCSC Ensembl
chr10:74938025..74939066hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg381042
hg191042
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv806n223
Supporting Variantsnssv18220663
Samples
Known GenesFAM149B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575819
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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