A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641236



Internal ID6681321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74228197..74229222hg38UCSC Ensembl
Innerchr17:74228209..74229210hg38UCSC Ensembl
Outerchr17:74228185..74229234hg38UCSC Ensembl
chr17:72224336..72225361hg19UCSC Ensembl
Innerchr17:72224348..72225349hg19UCSC Ensembl
Outerchr17:72224324..72225373hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381026
hg191026
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15738897
SamplesHG02787
Known GenesTTYH2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641236
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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