A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587830



Internal ID20960901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8085959..8086489hg38UCSC Ensembl
chr12:8238555..8239085hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38531
hg19531
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1378n223
Supporting Variantsnssv18229945
Samples
Known GenesNECAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587830
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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