A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586515



Internal ID6626827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77109467..77113856hg38UCSC Ensembl
Innerchr1:77109468..77113855hg38UCSC Ensembl
Outerchr1:77109466..77113857hg38UCSC Ensembl
chr1:77575152..77579541hg19UCSC Ensembl
Innerchr1:77575153..77579540hg19UCSC Ensembl
Outerchr1:77575151..77579542hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg384390
hg194390
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9979375
SamplesHG04219
Known GenesPIGK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586515
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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