A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263376



Internal ID20830416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:101796217..101809022hg38UCSC Ensembl
chr4:102717374..102730179hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3812806
hg1912806
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557083
Supporting Variants
Samples
Known GenesBANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263376
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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