A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585560



Internal ID6973082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27578839..27583520hg38UCSC Ensembl
Innerchr1:27578854..27583506hg38UCSC Ensembl
Outerchr1:27578825..27583535hg38UCSC Ensembl
chr1:27905350..27910031hg19UCSC Ensembl
Innerchr1:27905365..27910017hg19UCSC Ensembl
Outerchr1:27905336..27910046hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg384682
hg194682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9894312
SamplesHG03922
Known GenesAHDC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585560
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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