A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549541



Internal ID20922702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40537526..40538174hg38UCSC Ensembl
chr1:41003198..41003846hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38649
hg19649
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250942
Samples
Known GenesZNF684
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549541
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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