A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585611



Internal ID6973132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:29726995..29731160hg38UCSC Ensembl
Innerchr1:29727045..29731110hg38UCSC Ensembl
Outerchr1:29726911..29731244hg38UCSC Ensembl
chr1:30199842..30204007hg19UCSC Ensembl
Innerchr1:30199892..30203957hg19UCSC Ensembl
Outerchr1:30199758..30204091hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg384166
hg194166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9895149, essv9895150, essv9895151
SamplesNA19446, NA19307, NA19347
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585611
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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