A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640051



Internal ID7026829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15027947..15074425hg38UCSC Ensembl
Innerchr17:15027947..15074425hg38UCSC Ensembl
Outerchr17:15027447..15074925hg38UCSC Ensembl
chr17:14931264..14977742hg19UCSC Ensembl
Innerchr17:14931264..14977742hg19UCSC Ensembl
Outerchr17:14930764..14978242hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3846479
hg1946479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15623554
SamplesHG03572
Known GenesCDRT7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640051
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