A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602962



Internal ID6989995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163549477..163552813hg38UCSC Ensembl
Innerchr4:163549548..163552743hg38UCSC Ensembl
Outerchr4:163549407..163552884hg38UCSC Ensembl
chr4:164470629..164473965hg19UCSC Ensembl
Innerchr4:164470700..164473895hg19UCSC Ensembl
Outerchr4:164470559..164474036hg19UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg383337
hg193337
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11674669
SamplesHG04098
Known GenesMARCH1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602962
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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