A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541132



Internal ID20914417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:112595027..113169872hg38UCSC Ensembl
chr1:113137649..113712494hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38574846
hg19574846
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247423
Samples
Known GenesAKR7A2P1, CAPZA1, FAM19A3, LOC100996251, LOC100996702, LRIG2, MOV10, PPM1J, RHOC, SLC16A1, SLC16A1-AS1, ST7L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541132
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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