A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611847



Internal ID6652062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2688293..2694228hg38UCSC Ensembl
chr7:2727927..2733862hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg385936
hg195936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12668526
SamplesNA18591
Known GenesAMZ1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611847
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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