A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3605841



Internal ID6992778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95876040..95877863hg38UCSC Ensembl
Innerchr5:95876040..95877863hg38UCSC Ensembl
Outerchr5:95875938..95878056hg38UCSC Ensembl
chr5:95211744..95213567hg19UCSC Ensembl
Innerchr5:95211744..95213567hg19UCSC Ensembl
Outerchr5:95211642..95213760hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg381824
hg191824
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11983090, essv11983086, essv11983087, essv11983088, essv11983089
SamplesNA19445, NA19451, NA18915, HG02497, HG01890
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3605841
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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