A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1637866



Internal ID12800985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156836757..156836809hg38UCSC Ensembl
chr1:156806549..156806601hg19UCSC Ensembl
chr1:155073173..155073225hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3853
hg1953
hg1853
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4046734
SamplesHuRef
Known GenesNTRK1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1637866
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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