A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247423



Internal ID20814463
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 StatusS
Merged Variantsnsv6541132
Supporting Variants
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)nssv18247423
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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