A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107171



Internal ID22016404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:20339429..21325188hg38UCSC Ensembl
chr22:20326952..21679477hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38985760
hg191352526
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649702
Samples
Known GenesAIFM3, BCRP2, CRKL, FAM230B, KLHL22, LOC400891, LOC729444, LZTR1, MED15, P2RX6, P2RX6P, PI4KA, PI4KAP1, POM121L4P, POM121L8P, RIMBP3, SCARF2, SERPIND1, SLC7A4, SNAP29, THAP7, THAP7-AS1, TMEM191A, TMEM191B, TUBA3FP, ZNF74
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107171
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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