A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3191515



Internal ID22342211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71316334..71316502hg38UCSC Ensembl
chr6:72026037..72026205hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7961n152
Supporting Variantsnssv14329271
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3191515
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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