A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15316872



Internal ID5318688
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637167
Supporting Variants
SamplesHG04100
Known GenesNTRK3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15316872
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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