A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584881



Internal ID20957952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:54170455..58863076hg38UCSC Ensembl
chr10:55930215..60622836hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg384692622
hg194692622
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222402
Samples
Known GenesBICC1, CISD1, FAM133CP, IPMK, MIR3924, MTRNR2L5, PCDH15, TFAM, UBE2D1, ZWINT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584881
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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