A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003148



Internal ID19092365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:194885911..194921104hg38UCSC Ensembl
Innerchr3:194606640..194641833hg19UCSC Ensembl
Innerchr3:196087929..196123122hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3835194
hg1935194
hg1835194
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3611375, nssv3611371, nssv3611373, nssv3611372, nssv3611374
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)nsv1003148
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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