A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641004



Internal ID6681089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63678188..63678540hg38UCSC Ensembl
Innerchr17:63678196..63678533hg38UCSC Ensembl
Outerchr17:63678181..63678548hg38UCSC Ensembl
chr17:61755548..61755900hg19UCSC Ensembl
Innerchr17:61755556..61755893hg19UCSC Ensembl
Outerchr17:61755541..61755908hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15722553
SamplesHG02537
Known GenesMAP3K3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641004
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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