A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11527639



Internal ID1529455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87422870..87515781hg38UCSC Ensembl
chr4:88344022..88436933hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3892912
hg1992912
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3601276
Supporting Variants
SamplesHG03240
Known GenesNUDT9, SPARCL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11527639
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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