A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3176599



Internal ID22333960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43834868..43834937hg38UCSC Ensembl
chr7:43874467..43874536hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14435873
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3176599
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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