A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614823



Internal ID7001716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121521702..121540037hg38UCSC Ensembl
Innerchr7:121521752..121539987hg38UCSC Ensembl
Outerchr7:121521538..121540201hg38UCSC Ensembl
chr7:121161756..121180091hg19UCSC Ensembl
Innerchr7:121161806..121180041hg19UCSC Ensembl
Outerchr7:121161592..121180255hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3818336
hg1918336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12948194, essv12948191, essv12948192, essv12948190, essv12948193
SamplesHG00608, NA18947, NA19089, NA18968, NA18623
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614823
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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