A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12457604



Internal ID6134336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88414258..88435959hg38UCSC Ensembl
Innerchr6:88414258..88435959hg38UCSC Ensembl
Outerchr6:88413758..88436459hg38UCSC Ensembl
chr6:89123977..89145678hg19UCSC Ensembl
Innerchr6:89123977..89145678hg19UCSC Ensembl
Outerchr6:89123477..89146178hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3821702
hg1921702
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3609883
Supporting Variants
SamplesNA19669
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12457604
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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