A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1001887



Internal ID7067005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:97361314..97364135hg38UCSC Ensembl
Outerchr7:96990626..96993447hg19UCSC Ensembl
Outerchr7:96828562..96831383hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg382822
hg192822
hg182822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564270
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1001887
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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