A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547912



Internal ID20921112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:212938678..212939365hg38UCSC Ensembl
chr2:213803402..213804089hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38688
hg19688
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258642
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547912
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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