A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640529



Internal ID7027304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38678894..38681175hg38UCSC Ensembl
Innerchr17:38678934..38681135hg38UCSC Ensembl
Outerchr17:38678854..38681215hg38UCSC Ensembl
chr17:36835147..36837428hg19UCSC Ensembl
Innerchr17:36835187..36837388hg19UCSC Ensembl
Outerchr17:36835107..36837468hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg382282
hg192282
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15673183
SamplesHG03225
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640529
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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