A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004923



Internal ID19094140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162153428..162239146hg38UCSC Ensembl
Innerchr3:161871216..161956934hg19UCSC Ensembl
Innerchr3:163353910..163439628hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3885719
hg1985719
hg1885719
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4932n100
Supporting Variantsnssv3607925, nssv3607927, nssv3607924, nssv3607926, nssv3607923
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)nsv1004923
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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