A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613747



Internal ID6653955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75972331..75974204hg38UCSC Ensembl
Innerchr7:75972331..75974204hg38UCSC Ensembl
Outerchr7:75972214..75974307hg38UCSC Ensembl
chr7:75601649..75603522hg19UCSC Ensembl
Innerchr7:75601649..75603522hg19UCSC Ensembl
Outerchr7:75601532..75603625hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381874
hg191874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12848276
SamplesHG02134
Known GenesPOR
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613747
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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