A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526724



Internal ID22396107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25106560..25107633hg38UCSC Ensembl
chr12:25259494..25260567hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg381074
hg191074
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14361644, nssv14361642, nssv14361640, nssv14361641, nssv14361643
SamplesHG00512, HG00732, HG00733, HG00513, HG00514
Known GenesLRMP
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Commentscomplex variant
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526724
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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