A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544202



Internal ID20917441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36299204..36299796hg38UCSC Ensembl
chr1:36764805..36765397hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38593
hg19593
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251054
Samples
Known GenesTHRAP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544202
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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