A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608807



Internal ID6649040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42910163..42924856hg38UCSC Ensembl
Innerchr6:42910663..42924356hg38UCSC Ensembl
Outerchr6:42909163..42925856hg38UCSC Ensembl
chr6:42877901..42892594hg19UCSC Ensembl
Innerchr6:42878401..42892094hg19UCSC Ensembl
Outerchr6:42876901..42893594hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3814694
hg1914694
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12329454
SamplesHG02238
Known GenesPTCRA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608807
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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