A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637645



Internal ID6677748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3021600..3057596hg38UCSC Ensembl
chr16:3071601..3107597hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3835997
hg1935997
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15362842
SamplesHG02282
Known GenesCCDC64B, HCFC1R1, LOC100128770, MMP25, THOC6, TNFRSF12A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637645
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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