A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12460044



Internal ID2238984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90096164..90100075hg38UCSC Ensembl
Innerchr6:90096171..90100068hg38UCSC Ensembl
Outerchr6:90096157..90100082hg38UCSC Ensembl
chr6:90805883..90809794hg19UCSC Ensembl
Innerchr6:90805890..90809787hg19UCSC Ensembl
Outerchr6:90805876..90809801hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg383912
hg193912
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3609915
Supporting Variants
SamplesHG02010
Known GenesBACH2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12460044
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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