A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576249



Internal ID20949320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:15511675..15512889hg38UCSC Ensembl
chr12:15664609..15665823hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg381215
hg191215
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221656
Samples
Known GenesPTPRO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576249
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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