A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6051946



Internal ID9907139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:37418531..37422572hg38UCSC Ensembl
Outerchr17:37418060..37422992hg38UCSC Ensembl
Innerchr17:35778616..35782672hg19UCSC Ensembl
Outerchr17:35778145..35783092hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg384933
hg194948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670293
Supporting Variants
SamplesNA20802
Known GenesTADA2A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6051946
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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