A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3175385



Internal ID22333333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7856597..7856660hg38UCSC Ensembl
chr1:7916657..7916720hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv91n152
Supporting Variantsnssv14440066
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3175385
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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