A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601046



Internal ID6641304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76172675..76176770hg38UCSC Ensembl
Innerchr4:76172687..76176759hg38UCSC Ensembl
Outerchr4:76172664..76176782hg38UCSC Ensembl
chr4:77093828..77097923hg19UCSC Ensembl
Innerchr4:77093840..77097912hg19UCSC Ensembl
Outerchr4:77093817..77097935hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg384096
hg194096
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11508226
SamplesNA18978
Known GenesSCARB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601046
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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