A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641258



Internal ID7028032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75107625..75120521hg38UCSC Ensembl
Innerchr17:75107675..75120471hg38UCSC Ensembl
Outerchr17:75107564..75120582hg38UCSC Ensembl
chr17:73103720..73116616hg19UCSC Ensembl
Innerchr17:73103770..73116566hg19UCSC Ensembl
Outerchr17:73103659..73116677hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3812897
hg1912897
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15740525
SamplesNA11881
Known GenesARMC7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641258
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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