A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6134727



Internal ID9112130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77487633..77487677hg38UCSC Ensembl
Outerchr17:77487476..77487830hg38UCSC Ensembl
Innerchr17:75483715..75483759hg19UCSC Ensembl
Outerchr17:75483558..75483912hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2667045
Supporting Variants
SamplesNA19102
Known GenesSEPT9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6134727
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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