A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639451



Internal ID7026232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85032392..85054636hg38UCSC Ensembl
Innerchr16:85032892..85054136hg38UCSC Ensembl
Outerchr16:85031392..85055636hg38UCSC Ensembl
chr16:85065998..85088242hg19UCSC Ensembl
Innerchr16:85066498..85087742hg19UCSC Ensembl
Outerchr16:85064998..85089242hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3822245
hg1922245
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15547116
SamplesHG00421
Known GenesKIAA0513
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639451
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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