A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601398



Internal ID6988436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:92355727..92545688hg38UCSC Ensembl
chr4:93276878..93466839hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38189962
hg19189962
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11537178
SamplesHG03871
Known GenesGRID2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601398
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