A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9896448



Internal ID1555085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32619376..32622884hg38UCSC Ensembl
Innerchr1:32619388..32622872hg38UCSC Ensembl
Outerchr1:32619364..32622896hg38UCSC Ensembl
chr1:33084977..33088485hg19UCSC Ensembl
Innerchr1:33084989..33088473hg19UCSC Ensembl
Outerchr1:33084965..33088497hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg383509
hg193509
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585673
Supporting Variants
SamplesHG01438
Known GenesZBTB8OS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9896448
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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