A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537515



Internal ID20910849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:69648607..69649067hg38UCSC Ensembl
chr2:69875739..69876199hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg38461
hg19461
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258898
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537515
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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