A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3176127



Internal ID22333725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77094086..77094244hg38UCSC Ensembl
chr1:77559771..77559929hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14440581
SamplesHG00733
Known GenesPIGK
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3176127
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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