A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062506



Internal ID19151725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:60801204..60827446hg38UCSC Ensembl
Innerchr18:58468437..58494679hg19UCSC Ensembl
Innerchr18:56619417..56645659hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3826243
hg1926243
hg1826243
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3375n100
Supporting Variantsnssv3565621
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062506
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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