A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3606101



Internal ID18557696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141508683..141581880hg38UCSC Ensembl
Innerchr3:141227525..141300722hg19UCSC Ensembl
Innerchr3:142710215..142783412hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3873198
hg1973198
hg1873198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006237
Supporting Variants
Samples
Known GenesRASA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3606101
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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