A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600995



Internal ID6641253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:73399883..73404180hg38UCSC Ensembl
Innerchr4:73399883..73404180hg38UCSC Ensembl
Outerchr4:73399723..73404392hg38UCSC Ensembl
chr4:74265600..74269897hg19UCSC Ensembl
Innerchr4:74265600..74269897hg19UCSC Ensembl
Outerchr4:74265440..74270109hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg384298
hg194298
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11501055, essv11501056
SamplesHG02541, HG00324
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600995
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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