A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624000



Internal ID7010856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:82647146..82671167hg38UCSC Ensembl
chr10:84406902..84430923hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3824022
hg1924022
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv155e214
Supporting Variantsessv13879191, essv13879190, essv13879188, essv13879189, essv13879192, essv13879186, essv13879187
SamplesHG00323, HG01360, HG01345, HG00128, NA06994, HG01302, HG01507
Known GenesNRG3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624000
Frequency
Sample Size2504
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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