A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254591



Internal ID20821631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:151746038..156373752hg38UCSC Ensembl
chr2:152602552..157230264hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg384627715
hg194627713
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545135
Supporting Variants
Samples
Known GenesARL5A, ARL6IP6, CACNB4, FMNL2, GALNT13, KCNJ3, LOC100144595, NR4A2, PRPF40A, RPRM, STAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254591
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00067


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