A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15578168



Internal ID6324632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:955606..957738hg38UCSC Ensembl
Innerchr17:956106..957238hg38UCSC Ensembl
Outerchr17:954606..958738hg38UCSC Ensembl
chr17:858846..860978hg19UCSC Ensembl
Innerchr17:859346..860478hg19UCSC Ensembl
Outerchr17:857846..861978hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg382133
hg192133
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639663
Supporting Variants
SamplesNA19921
Known GenesNXN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15578168
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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