A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010897



Internal ID19100114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:99941910..100185939hg38UCSC Ensembl
Innerchr3:99660754..99904783hg19UCSC Ensembl
Innerchr3:101143444..101387473hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38244030
hg19244030
hg18244030
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4829n100
Supporting Variantsnssv3604231
Samples
Known GenesCMSS1, FILIP1L, MIR3921, MIR548G, TMEM30C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010897
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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