A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11641049



Internal ID2842937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145007989..145016351hg38UCSC Ensembl
chr4:145929141..145937503hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg388363
hg198363
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602551
Supporting Variants
SamplesHG02508
Known GenesANAPC10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11641049
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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