A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601397



Internal ID6988435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:92311963..92316725hg38UCSC Ensembl
Innerchr4:92311965..92316724hg38UCSC Ensembl
Outerchr4:92311962..92316727hg38UCSC Ensembl
chr4:93233114..93237876hg19UCSC Ensembl
Innerchr4:93233116..93237875hg19UCSC Ensembl
Outerchr4:93233113..93237878hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg384763
hg194763
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11537175, essv11537174, essv11537173, essv11537172, essv11537177, essv11537176, essv11537171
SamplesNA19394, NA20321, NA20320, NA19327, HG00551, NA19042, NA19037
Known GenesGRID2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601397
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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