A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6526467



Internal ID9503871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:11489047..11864608hg38UCSC Ensembl
Outerchr3:11489013..11864643hg38UCSC Ensembl
Innerchr3:11530521..11906082hg19UCSC Ensembl
Outerchr3:11530487..11906117hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg38375631
hg19375631
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677845
Supporting Variants
SamplesNA12341
Known GenesATG7, TAMM41, VGLL4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6526467
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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