A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563912



Internal ID20936983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7255565..7471608hg38UCSC Ensembl
chr5:7255678..7471721hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38216044
hg19216044
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267052
Samples
Known GenesADCY2, LOC442132, MIR4454
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563912
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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