A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564096



Internal ID18862377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:8270683..8421251hg38UCSC Ensembl
Innerchr18:8270681..8421249hg19UCSC Ensembl
Innerchr18:8260681..8411249hg18UCSC Ensembl
Cytoband18p11.23
Allele length
AssemblyAllele length
hg38150569
hg19150569
hg18150569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058445
Supporting Variants
Samples
Known GenesLOC100192426, PTPRM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564096
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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