A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005330



Internal ID7070426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:64854816..64857853hg38UCSC Ensembl
Outerchr7:64315194..64318231hg19UCSC Ensembl
Outerchr7:63952629..63955666hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg383038
hg193038
hg183038
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564349
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005330
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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