A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536402



Internal ID20909750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206452871..206452947hg38UCSC Ensembl
chr1:206626215..206626293hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3877
hg1979
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249999
Samples
Known GenesSRGAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536402
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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