A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15664516



Internal ID721167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35353525..35442202hg38UCSC Ensembl
Innerchr17:35353675..35442052hg38UCSC Ensembl
Outerchr17:35353375..35442352hg38UCSC Ensembl
chr17:33680544..33769221hg19UCSC Ensembl
Innerchr17:33680694..33769071hg19UCSC Ensembl
Outerchr17:33680394..33769371hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3888678
hg1988678
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640447
Supporting Variants
SamplesHG00338
Known GenesSLFN11, SLFN12, SLFN13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15664516
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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