A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585328



Internal ID6972852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16032246..16046354hg38UCSC Ensembl
Innerchr1:16032248..16046352hg38UCSC Ensembl
Outerchr1:16032244..16046356hg38UCSC Ensembl
chr1:16358741..16372849hg19UCSC Ensembl
Innerchr1:16358743..16372847hg19UCSC Ensembl
Outerchr1:16358739..16372851hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3814109
hg1914109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9864869, essv9864867, essv9864868
SamplesNA19471, NA18573, NA19003
Known GenesCLCNKA, CLCNKB
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585328
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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