A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5909589



Internal ID9609549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149480791..149481750hg38UCSC Ensembl
chr6:149801927..149802886hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38960
hg19960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670181
Supporting Variants
SamplesNA19311
Known GenesZC3H12D
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5909589
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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