A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624849



Internal ID7011699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126058586..126117243hg38UCSC Ensembl
chr10:127747155..127805812hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3858658
hg1958658
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13964375
SamplesHG01708
Known GenesADAM12
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624849
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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