A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12461380



Internal ID839439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90416288..90436562hg38UCSC Ensembl
Innerchr6:90416288..90436562hg38UCSC Ensembl
Outerchr6:90415788..90437062hg38UCSC Ensembl
chr6:91126007..91146281hg19UCSC Ensembl
Innerchr6:91126007..91146281hg19UCSC Ensembl
Outerchr6:91125507..91146781hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3820275
hg1920275
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3609923
Supporting Variants
SamplesHG00436
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12461380
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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