A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546482



Internal ID20875525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7187356..8831900hg38UCSC Ensembl
chr1:7247416..8891959hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg381644545
hg191644544
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251377
Samples
Known GenesCAMTA1, ERRFI1, PARK7, PER3, RERE, SLC45A1, TNFRSF9, UTS2, VAMP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546482
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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