A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11984555



Internal ID6177034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:97387012..97390863hg38UCSC Ensembl
Innerchr5:97387012..97390863hg38UCSC Ensembl
Outerchr5:97386917..97390924hg38UCSC Ensembl
chr5:96722716..96726567hg19UCSC Ensembl
Innerchr5:96722716..96726567hg19UCSC Ensembl
Outerchr5:96722621..96726628hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg383852
hg193852
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3605877
Supporting Variants
SamplesNA19713
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11984555
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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