A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585289



Internal ID6972814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14780652..14820893hg38UCSC Ensembl
Innerchr1:14780665..14820880hg38UCSC Ensembl
Outerchr1:14780639..14820906hg38UCSC Ensembl
chr1:15107148..15147389hg19UCSC Ensembl
Innerchr1:15107161..15147376hg19UCSC Ensembl
Outerchr1:15107135..15147402hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3840242
hg1940242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9863412
SamplesHG03372
Known GenesKAZN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585289
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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