A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637652



Internal ID7024443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3095742..3096843hg38UCSC Ensembl
Innerchr16:3095787..3096799hg38UCSC Ensembl
Outerchr16:3095698..3096888hg38UCSC Ensembl
chr16:3145743..3146844hg19UCSC Ensembl
Innerchr16:3145788..3146800hg19UCSC Ensembl
Outerchr16:3145699..3146889hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381102
hg191102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15362863
SamplesHG02142
Known GenesZSCAN10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637652
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