A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6030607



Internal ID9678296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:52113425..52116639hg38UCSC Ensembl
Outerchr16:52113388..52116689hg38UCSC Ensembl
Innerchr16:52147337..52150551hg19UCSC Ensembl
Outerchr16:52147300..52150601hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg383302
hg193302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662487
Supporting Variants
SamplesNA19429
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6030607
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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