A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620653



Internal ID6660834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72924157..73079106hg38UCSC Ensembl
chr9:75539073..75694022hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38154950
hg19154950
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13517108
SamplesHG00276
Known GenesALDH1A1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620653
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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