A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6561656



Internal ID9716828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:73003476..73005399hg38UCSC Ensembl
chr16:73037375..73039298hg19UCSC Ensembl
Cytoband16q22.3
Allele length
AssemblyAllele length
hg381924
hg191924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672800
Supporting Variants
SamplesNA19469
Known GenesZFHX3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6561656
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