A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057565



Internal ID18800096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:80199442..80257174hg38UCSC Ensembl
Innerchr18:77957325..78015057hg19UCSC Ensembl
Innerchr18:76058316..76116029hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3857733
hg1957733
hg1857714
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3417n100
Supporting Variantsnssv3563111
Samples
Known GenesPARD6G
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057565
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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