A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585324



Internal ID6972848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15985475..16003587hg38UCSC Ensembl
Innerchr1:15985625..16003437hg38UCSC Ensembl
Outerchr1:15985325..16003737hg38UCSC Ensembl
chr1:16311970..16330082hg19UCSC Ensembl
Innerchr1:16312120..16329932hg19UCSC Ensembl
Outerchr1:16311820..16330232hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3818113
hg1918113
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9864707
SamplesHG03792
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585324
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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