A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549532



Internal ID20922693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:227777056..227779316hg38UCSC Ensembl
chr1:227964757..227967017hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg382261
hg192261
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250306
Samples
Known GenesSNAP47
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549532
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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