A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998101



Internal ID19157638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:154573259..154727150hg38UCSC Ensembl
Innerchr3:154291048..154444939hg19UCSC Ensembl
Innerchr3:155773742..155927633hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38153892
hg19153892
hg18153892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4925n100
Supporting Variantsnssv3606348, nssv3606347, nssv3606351, nssv3606349, nssv3606350
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)nsv998101
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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