A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3204896



Internal ID22353675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124609433..124611943hg38UCSC Ensembl
chr10:126298002..126300512hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg382511
hg192511
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14412791, nssv14412790
SamplesHG00514
Known GenesLHPP
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3204896
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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