A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640185



Internal ID6680272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19907274..19908881hg38UCSC Ensembl
Innerchr17:19907275..19908880hg38UCSC Ensembl
Outerchr17:19907273..19908882hg38UCSC Ensembl
chr17:19810587..19812194hg19UCSC Ensembl
Innerchr17:19810588..19812193hg19UCSC Ensembl
Outerchr17:19810586..19812195hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381608
hg191608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15648074, essv15648072, essv15648073
SamplesHG02582, HG03063, HG02805
Known GenesAKAP10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640185
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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