A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622437



Internal ID6662607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15121111..15124207hg38UCSC Ensembl
Innerchr10:15121171..15124147hg38UCSC Ensembl
Outerchr10:15121051..15124267hg38UCSC Ensembl
chr10:15163110..15166206hg19UCSC Ensembl
Innerchr10:15163170..15166146hg19UCSC Ensembl
Outerchr10:15163050..15166266hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg383097
hg193097
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13704060, essv13704062, essv13704061
SamplesHG00457, NA18538, HG02064
Known GenesNMT2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622437
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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