A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602153



Internal ID6989187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:127854814..127857400hg38UCSC Ensembl
Innerchr4:127854814..127857400hg38UCSC Ensembl
Outerchr4:127854488..127857699hg38UCSC Ensembl
chr4:128775969..128778555hg19UCSC Ensembl
Innerchr4:128775969..128778555hg19UCSC Ensembl
Outerchr4:128775643..128778854hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg382587
hg192587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11596601
SamplesNA18534
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602153
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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