A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613743



Internal ID6653951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75917905..75929949hg38UCSC Ensembl
Innerchr7:75917905..75929949hg38UCSC Ensembl
Outerchr7:75917405..75930449hg38UCSC Ensembl
chr7:75547223..75559267hg19UCSC Ensembl
Innerchr7:75547223..75559267hg19UCSC Ensembl
Outerchr7:75546723..75559767hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3812045
hg1912045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12848231
SamplesHG02219
Known GenesPOR
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613743
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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