A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891219



Internal ID19185615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143728268..143740341hg38UCSC Ensembl
Outerchr7:143728268..143740341hg38UCSC Ensembl
Innerchr7:143425361..143437434hg19UCSC Ensembl
Outerchr7:143425361..143437434hg19UCSC Ensembl
Innerchr7:143056294..143068367hg18UCSC Ensembl
Outerchr7:143056294..143068367hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3812074
hg1912074
hg1812074
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797938, essv25797598
Samples
Known GenesFAM115C
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891219
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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