A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641337



Internal ID7028111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78606754..78607865hg38UCSC Ensembl
Innerchr17:78606754..78607865hg38UCSC Ensembl
Outerchr17:78606589..78607976hg38UCSC Ensembl
chr17:76602836..76603947hg19UCSC Ensembl
Innerchr17:76602836..76603947hg19UCSC Ensembl
Outerchr17:76602671..76604058hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg381112
hg191112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15753142, essv15753143
SamplesHG03965, HG03826
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641337
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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