A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599987



Internal ID6987031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26441158..26452552hg38UCSC Ensembl
Innerchr4:26441158..26452552hg38UCSC Ensembl
Outerchr4:26440833..26452858hg38UCSC Ensembl
chr4:26442780..26454174hg19UCSC Ensembl
Innerchr4:26442780..26454174hg19UCSC Ensembl
Outerchr4:26442455..26454480hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3811395
hg1911395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11375561, essv11375569, essv11375564, essv11375562, essv11375565, essv11375560, essv11375566, essv11375570, essv11375572, essv11375571, essv11375568, essv11375573, essv11375563, essv11375567
SamplesHG03115, NA18504, HG03139, NA18498, HG03189, HG02946, HG02943, NA19236, HG02429, HG02923, HG02974, NA19185, NA18488, HG03265
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599987
Frequency
Sample Size2504
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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