A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222814



Internal ID20789854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46746954..47593429hg38UCSC Ensembl
chr10:48180788..48946356hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38846476
hg19765569
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586608
Supporting Variants
Samples
Known GenesAGAP9, ANXA8, BMS1P1, BMS1P2, BMS1P5, BMS1P6, FAM25C, FAM25G, FRMPD2P1, GDF10, GDF2, PTPN20A, PTPN20B, RBP3, ZNF488
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222814
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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