A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7442246



Internal ID10720528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:835694..836004hg38UCSC Ensembl
Outerchr17:738934..739244hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3172679
Supporting Variants
SamplesHuRef
Known GenesNXN
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7442246
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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