A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615741



Internal ID6655939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:158774147..159247998hg38UCSC Ensembl
Innerchr7:158774297..159247848hg38UCSC Ensembl
Outerchr7:158773997..159248148hg38UCSC Ensembl
chr7:158566838..159040688hg19UCSC Ensembl
Innerchr7:158566988..159040538hg19UCSC Ensembl
Outerchr7:158566688..159040838hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38473852
hg19473851
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13053716
SamplesHG03851
Known GenesESYT2, LINC00689, VIPR2, WDR60
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615741
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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