A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5635862



Internal ID8939617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:16405902..16410408hg38UCSC Ensembl
Outerchr17:16405531..16410778hg38UCSC Ensembl
Innerchr17:16309216..16313722hg19UCSC Ensembl
Outerchr17:16308845..16314092hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg385248
hg195248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv2673996
Supporting Variants
SamplesHG00464
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5635862
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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