A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891085



Internal ID19185481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:20438825..20480470hg38UCSC Ensembl
Outerchr7:20435721..20496241hg38UCSC Ensembl
Innerchr7:20478448..20520093hg19UCSC Ensembl
Outerchr7:20475344..20535864hg19UCSC Ensembl
Innerchr7:20444973..20486618hg18UCSC Ensembl
Outerchr7:20441869..20502389hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3860521
hg1960521
hg1860521
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798002, essv25782120, essv25780218, essv25783118, essv25778643, essv25785297, essv25781853, essv25797115, essv25784790, essv25796132, essv25783995, essv25783662, essv25797710, essv25778388
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891085
Frequency
Sample Size3017
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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