A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555195



Internal ID20928285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:69705835..69706569hg38UCSC Ensembl
chr2:69932967..69933701hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg38735
hg19735
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3919n223
Supporting Variantsnssv18258907
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555195
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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