A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608070



Internal ID6995000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10352508..10356808hg38UCSC Ensembl
Innerchr6:10352508..10356808hg38UCSC Ensembl
Outerchr6:10352193..10356827hg38UCSC Ensembl
chr6:10352741..10357041hg19UCSC Ensembl
Innerchr6:10352741..10357041hg19UCSC Ensembl
Outerchr6:10352426..10357060hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg384301
hg194301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12188372
SamplesNA20885
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608070
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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