A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623209



Internal ID6663377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50511739..50518176hg38UCSC Ensembl
Innerchr10:50511746..50518170hg38UCSC Ensembl
Outerchr10:50511733..50518183hg38UCSC Ensembl
chr10:52271499..52277936hg19UCSC Ensembl
Innerchr10:52271506..52277930hg19UCSC Ensembl
Outerchr10:52271493..52277943hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg386438
hg196438
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13803076
SamplesNA20318
Known GenesSGMS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623209
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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