A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564349



Internal ID7035449
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1005330
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564349
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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