A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6016601



Internal ID9522197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:82984140..82984282hg38UCSC Ensembl
Outerchr17:82984092..82984359hg38UCSC Ensembl
Innerchr17:80942016..80942158hg19UCSC Ensembl
Outerchr17:80941968..80942235hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2670486
Supporting Variants
SamplesNA19010
Known GenesB3GNTL1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6016601
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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