A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595255



Internal ID6635529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9879400..9888341hg38UCSC Ensembl
Innerchr3:9879415..9888326hg38UCSC Ensembl
Outerchr3:9879385..9888356hg38UCSC Ensembl
chr3:9921084..9930025hg19UCSC Ensembl
Innerchr3:9921099..9930010hg19UCSC Ensembl
Outerchr3:9921069..9930040hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg388942
hg198942
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10918318, essv10918324, essv10918315, essv10918321, essv10918308, essv10918314, essv10918323, essv10918310, essv10918313, essv10918320, essv10918319, essv10918311, essv10918309, essv10918312, essv10918316, essv10918322, essv10918317
SamplesHG00729, HG01802, HG00449, HG01809, HG02016, HG02374, HG02082, NA18973, HG01595, HG02141, HG00623, NA18943, HG02019, HG02371, HG01600, HG02186, HG02406
Known GenesCIDEC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595255
Frequency
Sample Size2504
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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