A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891009



Internal ID19185405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1467375..1513737hg38UCSC Ensembl
Outerchr7:1467375..1513737hg38UCSC Ensembl
Innerchr7:1507011..1553373hg19UCSC Ensembl
Outerchr7:1507011..1553373hg19UCSC Ensembl
Innerchr7:1473537..1519899hg18UCSC Ensembl
Outerchr7:1473537..1519899hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3846363
hg1946363
hg1846363
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780662
Samples
Known GenesINTS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891009
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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