A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645735



Internal ID7032483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36415120..36427559hg38UCSC Ensembl
Innerchr20:36415620..36427059hg38UCSC Ensembl
Outerchr20:36414120..36428559hg38UCSC Ensembl
chr20:35043523..35055962hg19UCSC Ensembl
Innerchr20:35044023..35055462hg19UCSC Ensembl
Outerchr20:35042523..35056962hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3812440
hg1912440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16179785, essv16179782, essv16179786, essv16179792, essv16179795, essv16179781, essv16179784, essv16179789, essv16179783, essv16179791, essv16179796, essv16179787, essv16179794, essv16179788, essv16179797, essv16179793, essv16179790, essv16179798
SamplesHG02250, HG00766, HG02029, HG02058, HG02394, HG02155, HG01816, HG00632, HG02070, HG02086, HG00607, NA18591, HG02188, HG02371, HG02133, HG00421, HG01846, HG02186
Known GenesDLGAP4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645735
Frequency
Sample Size2504
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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