A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641412



Internal ID7028186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:82004756..82015461hg38UCSC Ensembl
chr17:79962632..79973337hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3810706
hg1910706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15764847, essv15764846, essv15764848
SamplesNA12815, NA18747, NA18939
Known GenesASPSCR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641412
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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