A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599767



Internal ID6986812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16903902..16904607hg38UCSC Ensembl
Innerchr4:16903933..16904577hg38UCSC Ensembl
Outerchr4:16903872..16904638hg38UCSC Ensembl
chr4:16905525..16906230hg19UCSC Ensembl
Innerchr4:16905556..16906200hg19UCSC Ensembl
Outerchr4:16905495..16906261hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38706
hg19706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11360423
SamplesHG02337
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599767
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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