A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15346842



Internal ID2695345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100135346..100237690hg38UCSC Ensembl
Innerchr15:100135408..100237628hg38UCSC Ensembl
Outerchr15:100135284..100237752hg38UCSC Ensembl
chr15:100675551..100777895hg19UCSC Ensembl
Innerchr15:100675613..100777833hg19UCSC Ensembl
Outerchr15:100675489..100777957hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38102345
hg19102345
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637468
Supporting Variants
SamplesHG02384
Known GenesADAMTS17
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15346842
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer