A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891062



Internal ID18838772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:14107205..14149743hg38UCSC Ensembl
Outerchr7:14077492..14173007hg38UCSC Ensembl
Innerchr7:14146830..14189368hg19UCSC Ensembl
Outerchr7:14117117..14212632hg19UCSC Ensembl
Innerchr7:14113355..14155893hg18UCSC Ensembl
Outerchr7:14083642..14179157hg18UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3895516
hg1995516
hg1895516
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781506, essv25788940
Samples
Known GenesDGKB
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891062
Frequency
Sample Size3017
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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