A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601062



Internal ID6641320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76709043..76726281hg38UCSC Ensembl
Innerchr4:76709073..76726251hg38UCSC Ensembl
Outerchr4:76709013..76726311hg38UCSC Ensembl
chr4:77630196..77647434hg19UCSC Ensembl
Innerchr4:77630226..77647404hg19UCSC Ensembl
Outerchr4:77630166..77647464hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3817239
hg1917239
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11508309
SamplesHG02382
Known GenesSHROOM3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601062
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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