A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602608



Internal ID6642864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147742992..147755464hg38UCSC Ensembl
Innerchr4:147742992..147755464hg38UCSC Ensembl
Outerchr4:147742492..147755964hg38UCSC Ensembl
chr4:148664143..148676615hg19UCSC Ensembl
Innerchr4:148664143..148676615hg19UCSC Ensembl
Outerchr4:148663643..148677115hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg3812473
hg1912473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11648380
SamplesHG00610
Known GenesARHGAP10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602608
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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