A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15363709



Internal ID5365525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4353267..4362846hg38UCSC Ensembl
Innerchr16:4353267..4362846hg38UCSC Ensembl
Outerchr16:4353058..4363084hg38UCSC Ensembl
chr16:4403268..4412847hg19UCSC Ensembl
Innerchr16:4403268..4412847hg19UCSC Ensembl
Outerchr16:4403059..4413085hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg389580
hg199580
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637696
Supporting Variants
SamplesNA19058
Known GenesCORO7, CORO7-PAM16
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15363709
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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