A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640123



Internal ID7026900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17120904..17122067hg38UCSC Ensembl
Innerchr17:17120904..17122067hg38UCSC Ensembl
Outerchr17:17120711..17122267hg38UCSC Ensembl
chr17:17024218..17025381hg19UCSC Ensembl
Innerchr17:17024218..17025381hg19UCSC Ensembl
Outerchr17:17024025..17025581hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381164
hg191164
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15633745, essv15633746
SamplesHG00663, NA18874
Known GenesMPRIP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640123
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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