A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585567



Internal ID6625884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27959203..27961869hg38UCSC Ensembl
Innerchr1:27959233..27961839hg38UCSC Ensembl
Outerchr1:27959173..27961899hg38UCSC Ensembl
chr1:28285714..28288380hg19UCSC Ensembl
Innerchr1:28285744..28288350hg19UCSC Ensembl
Outerchr1:28285684..28288410hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg382667
hg192667
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9894556
SamplesHG01598
Known GenesXKR8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585567
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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