A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612467



Internal ID6999368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:19371854..19386517hg38UCSC Ensembl
Innerchr7:19371857..19386514hg38UCSC Ensembl
Outerchr7:19371851..19386520hg38UCSC Ensembl
chr7:19411477..19426140hg19UCSC Ensembl
Innerchr7:19411480..19426137hg19UCSC Ensembl
Outerchr7:19411474..19426143hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3814664
hg1914664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12692806
SamplesHG01770
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612467
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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