A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615664



Internal ID7002553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156522845..156529154hg38UCSC Ensembl
Innerchr7:156522845..156529154hg38UCSC Ensembl
Outerchr7:156522642..156529302hg38UCSC Ensembl
chr7:156315539..156321848hg19UCSC Ensembl
Innerchr7:156315539..156321848hg19UCSC Ensembl
Outerchr7:156315336..156321996hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg386310
hg196310
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13039345
SamplesNA12058
Known GenesLINC01006
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615664
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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