A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13879191



Internal ID1632606
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624000
Supporting Variants
SamplesHG01507
Known GenesNRG3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13879191
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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