A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012607



Internal ID19101824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..63682hg38UCSC Ensembl
Innerchr3:60333..105365hg19UCSC Ensembl
Innerchr3:35333..80365hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3845028
hg1945033
hg1845033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4601n100
Supporting Variantsnssv3593509, nssv3593510
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)nsv1012607
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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