A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15735636



Internal ID1048693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72384195..72388365hg38UCSC Ensembl
Innerchr17:72384241..72388319hg38UCSC Ensembl
Outerchr17:72384149..72388411hg38UCSC Ensembl
chr17:70380336..70384506hg19UCSC Ensembl
Innerchr17:70380382..70384460hg19UCSC Ensembl
Outerchr17:70380290..70384552hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg384171
hg194171
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641196
Supporting Variants
SamplesHG00671
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15735636
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