A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14412371



Internal ID22314506
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 StatusS
Merged Variantsnsv3288929
Supporting Variants
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)nssv14412371
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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