A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608769



Internal ID6995693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:40275257..40280869hg38UCSC Ensembl
Innerchr6:40275307..40280819hg38UCSC Ensembl
Outerchr6:40275195..40280931hg38UCSC Ensembl
chr6:40242996..40248608hg19UCSC Ensembl
Innerchr6:40243046..40248558hg19UCSC Ensembl
Outerchr6:40242934..40248670hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg385613
hg195613
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12326746
SamplesHG02784
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608769
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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