A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5704325



Internal ID9879185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:98082452..98143095hg38UCSC Ensembl
Outerchr5:98082415..98143145hg38UCSC Ensembl
Innerchr5:97418156..97478799hg19UCSC Ensembl
Outerchr5:97418119..97478849hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3860731
hg1960731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672561
Supporting Variants
SamplesNA20753
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5704325
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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