A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536449



Internal ID20909796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169227760..169402827hg38UCSC Ensembl
chr1:169196998..169372065hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38175068
hg19175068
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248070
Samples
Known GenesBLZF1, CCDC181, NME7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536449
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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