A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12472465



Internal ID4011205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96213992..96215242hg38UCSC Ensembl
Innerchr6:96213992..96215242hg38UCSC Ensembl
Outerchr6:96213849..96215379hg38UCSC Ensembl
chr6:96661868..96663118hg19UCSC Ensembl
Innerchr6:96661868..96663118hg19UCSC Ensembl
Outerchr6:96661725..96663255hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg381251
hg191251
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3610070
Supporting Variants
SamplesHG03667
Known GenesFUT9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12472465
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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