A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641436



Internal ID7028210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:82659688..82666055hg38UCSC Ensembl
Innerchr17:82659738..82666005hg38UCSC Ensembl
Outerchr17:82659638..82666105hg38UCSC Ensembl
chr17:80617564..80623931hg19UCSC Ensembl
Innerchr17:80617614..80623881hg19UCSC Ensembl
Outerchr17:80617514..80623981hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg386368
hg196368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15770018
SamplesNA18579
Known GenesRAB40B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641436
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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