A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639942



Internal ID7026720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10710767..10713237hg38UCSC Ensembl
Innerchr17:10710767..10713237hg38UCSC Ensembl
Outerchr17:10710741..10713271hg38UCSC Ensembl
chr17:10614084..10616554hg19UCSC Ensembl
Innerchr17:10614084..10616554hg19UCSC Ensembl
Outerchr17:10614058..10616588hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg382471
hg192471
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15610873
SamplesHG01914
Known GenesADPRM
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639942
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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