A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6467127



Internal ID9444530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:156522170..156525949hg38UCSC Ensembl
Outerchr1:156522133..156525999hg38UCSC Ensembl
Innerchr1:156491962..156495741hg19UCSC Ensembl
Outerchr1:156491925..156495791hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg383867
hg193867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675734
Supporting Variants
SamplesHG00334
Known GenesIQGAP3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6467127
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