A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6462290



Internal ID9439693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:21675662..21683213hg38UCSC Ensembl
Outerchr6:21675625..21683263hg38UCSC Ensembl
Innerchr6:21675893..21683444hg19UCSC Ensembl
Outerchr6:21675856..21683494hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg387639
hg197639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678811
Supporting Variants
SamplesHG00653
Known GenesCASC15
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6462290
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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