A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637676



Internal ID6677778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3862016..3862420hg38UCSC Ensembl
Innerchr16:3862066..3862370hg38UCSC Ensembl
Outerchr16:3861947..3862489hg38UCSC Ensembl
chr16:3912017..3912421hg19UCSC Ensembl
Innerchr16:3912067..3912371hg19UCSC Ensembl
Outerchr16:3911948..3912490hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15363304, essv15363305
SamplesHG01867, HG01862
Known GenesCREBBP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637676
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