A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12604959



Internal ID3882144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157925184..157925937hg38UCSC Ensembl
Innerchr6:157925270..157925710hg38UCSC Ensembl
Outerchr6:157924964..157926157hg38UCSC Ensembl
chr6:158346216..158346969hg19UCSC Ensembl
Innerchr6:158346302..158346742hg19UCSC Ensembl
Outerchr6:158345996..158347189hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38754
hg19754
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3611386
Supporting Variants
SamplesHG03521
Known GenesSNX9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12604959
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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