A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6597475



Internal ID9538629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96911907..96922016hg38UCSC Ensembl
chr5:96247611..96257720hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3810110
hg1910110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658182
Supporting Variants
SamplesNA19068
Known GenesERAP2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6597475
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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