A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539649



Internal ID20912945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85021343..85023186hg38UCSC Ensembl
chr2:85248466..85250309hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg381844
hg191844
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259117
Samples
Known GenesKCMF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539649
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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