A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639754



Internal ID7026532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:3704982..3716205hg38UCSC Ensembl
Innerchr17:3704985..3716203hg38UCSC Ensembl
Outerchr17:3704980..3716208hg38UCSC Ensembl
chr17:3608276..3619499hg19UCSC Ensembl
Innerchr17:3608279..3619497hg19UCSC Ensembl
Outerchr17:3608274..3619502hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3811224
hg1911224
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15588627
SamplesHG02151
Known GenesITGAE
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639754
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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