A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637167



Internal ID6677274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88171191..88173977hg38UCSC Ensembl
Innerchr15:88171191..88173977hg38UCSC Ensembl
Outerchr15:88171006..88174176hg38UCSC Ensembl
chr15:88714422..88717208hg19UCSC Ensembl
Innerchr15:88714422..88717208hg19UCSC Ensembl
Outerchr15:88714237..88717407hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg382787
hg192787
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15316872
SamplesHG04100
Known GenesNTRK3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637167
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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