A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585173



Internal ID20958244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14217987..14218607hg38UCSC Ensembl
chr10:14259986..14260606hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38621
hg19621
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222300
Samples
Known GenesFRMD4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585173
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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