A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608129



Internal ID6648368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13525301..13607816hg38UCSC Ensembl
Innerchr6:13525313..13607804hg38UCSC Ensembl
Outerchr6:13525289..13607828hg38UCSC Ensembl
chr6:13525533..13608048hg19UCSC Ensembl
Innerchr6:13525545..13608036hg19UCSC Ensembl
Outerchr6:13525521..13608060hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3882516
hg1982516
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12193458
SamplesHG04177
Known GenesSIRT5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608129
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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