A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3288929



Internal ID22387346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71381602..71381715hg38UCSC Ensembl
chr6:72091305..72091418hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14412371
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3288929
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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