A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577657



Internal ID16365066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:75262352..75278318hg38UCSC Ensembl
Innerchr18:72974307..72990273hg19UCSC Ensembl
Innerchr18:71103295..71119261hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3815967
hg1915967
hg1815967
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150633
SamplesHGDP00894
Known GenesTSHZ1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577657
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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