A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614888



Internal ID7001781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:125097156..125134482hg38UCSC Ensembl
Innerchr7:125097180..125134458hg38UCSC Ensembl
Outerchr7:125097132..125134506hg38UCSC Ensembl
chr7:124737210..124774536hg19UCSC Ensembl
Innerchr7:124737234..124774512hg19UCSC Ensembl
Outerchr7:124737186..124774560hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3837327
hg1937327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12951344
SamplesHG02491
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614888
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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