A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264397



Internal ID20831437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169780525..178315900hg38UCSC Ensembl
chr4:170701676..179237054hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg388535376
hg198535379
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570050
Supporting Variants
Samples
Known GenesAADAT, ADAM29, AGA, ASB5, CEP44, FBXO8, GALNT7, GALNTL6, GLRA3, GPM6A, HAND2, HAND2-AS1, HMGB2, HPGD, LINC01098, LINC01099, LOC100506085, LOC100506122, MFAP3L, MIR4276, MIR6082, NEIL3, SAP30, SCRG1, SPATA4, SPCS3, VEGFC, WDR17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264397
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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