A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553253



Internal ID20926362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:70914185..70915080hg38UCSC Ensembl
chr2:71141315..71142210hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg38896
hg19896
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3923n223
Supporting Variantsnssv18258949
Samples
Known GenesVAX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553253
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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