A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577830



Internal ID20950901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8085933..8086481hg38UCSC Ensembl
chr12:8238529..8239077hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38549
hg19549
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1378n223
Supporting Variantsnssv18217340
Samples
Known GenesNECAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577830
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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