A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12457621



Internal ID4350906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88559943..88564385hg38UCSC Ensembl
Innerchr6:88559973..88564355hg38UCSC Ensembl
Outerchr6:88559913..88564415hg38UCSC Ensembl
chr6:89269662..89274104hg19UCSC Ensembl
Innerchr6:89269692..89274074hg19UCSC Ensembl
Outerchr6:89269632..89274134hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg384443
hg194443
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3609885
Supporting Variants
SamplesHG03887
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12457621
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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