A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251897



Internal ID20818937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86344291..89254074hg38UCSC Ensembl
chr1:86809974..89719757hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg382909784
hg192909784
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536739
Supporting Variants
Samples
Known GenesCCBL2, CLCA1, CLCA2, CLCA3P, CLCA4, GBP1, GBP2, GBP3, GBP4, GBP7, GTF2B, HS2ST1, LINC01140, LMO4, LOC100505768, MIR7856, ODF2L, PKN2, RBMXL1, SEP15, SH3GLB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251897
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00352


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