A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536816



Internal ID20910159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:180356052..180356686hg38UCSC Ensembl
chr1:180325187..180325821hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248859
Samples
Known GenesACBD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536816
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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