A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6387295



Internal ID9364698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32827726..32827903hg38UCSC Ensembl
chr6:32795503..32795680hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2660966
Supporting Variants
SamplesNA19819
Known GenesTAP2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6387295
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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