A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637165



Internal ID6677272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:87907200..87908096hg38UCSC Ensembl
Innerchr15:87907250..87908046hg38UCSC Ensembl
Outerchr15:87907105..87908191hg38UCSC Ensembl
chr15:88450431..88451327hg19UCSC Ensembl
Innerchr15:88450481..88451277hg19UCSC Ensembl
Outerchr15:88450336..88451422hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38897
hg19897
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15316735
SamplesHG04161
Known GenesNTRK3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637165
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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