A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612309



Internal ID6999210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14071351..14140649hg38UCSC Ensembl
Innerchr7:14071851..14140149hg38UCSC Ensembl
Outerchr7:14070351..14141649hg38UCSC Ensembl
chr7:14110976..14180274hg19UCSC Ensembl
Innerchr7:14111476..14179774hg19UCSC Ensembl
Outerchr7:14109976..14181274hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3869299
hg1969299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1269e214
Supporting Variantsessv12685458
SamplesNA20832
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612309
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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