A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552881



Internal ID20926002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52300523..52300867hg38UCSC Ensembl
chr1:52766195..52766539hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249711
Samples
Known GenesZFYVE9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552881
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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