A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601176



Internal ID6988215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82413420..82414961hg38UCSC Ensembl
Innerchr4:82413420..82414961hg38UCSC Ensembl
Outerchr4:82413049..82415251hg38UCSC Ensembl
chr4:83334573..83336114hg19UCSC Ensembl
Innerchr4:83334573..83336114hg19UCSC Ensembl
Outerchr4:83334202..83336404hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg381542
hg191542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11519994
SamplesNA19054
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601176
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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