A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601244



Internal ID6641501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:85624254..85650103hg38UCSC Ensembl
Innerchr4:85624254..85650103hg38UCSC Ensembl
Outerchr4:85623754..85650603hg38UCSC Ensembl
chr4:86545407..86571256hg19UCSC Ensembl
Innerchr4:86545407..86571256hg19UCSC Ensembl
Outerchr4:86544907..86571756hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg3825850
hg1925850
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11525002
SamplesHG01504
Known GenesARHGAP24
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601244
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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