A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15633745



Internal ID1045569
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640123
Supporting Variants
SamplesHG00663
Known GenesMPRIP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15633745
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer