A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611851



Internal ID6998753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2707441..2709674hg38UCSC Ensembl
Innerchr7:2707441..2709674hg38UCSC Ensembl
Outerchr7:2707324..2709743hg38UCSC Ensembl
chr7:2747075..2749308hg19UCSC Ensembl
Innerchr7:2747075..2749308hg19UCSC Ensembl
Outerchr7:2746958..2749377hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg382234
hg192234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12668855, essv12668854
SamplesHG01063, NA19138
Known GenesAMZ1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611851
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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