A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169610



Internal ID21313421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:159889156..159930826hg38UCSC Ensembl
Outerchr3:159881422..159933133hg38UCSC Ensembl
Innerchr3:159606945..159648615hg19UCSC Ensembl
Outerchr3:159599211..159650921hg19UCSC Ensembl
Innerchr3:161089639..161131309hg18UCSC Ensembl
Outerchr3:161081905..161133615hg18UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg3851712
hg1951711
hg1851711
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247586, nssv14248270
SamplesNGO_30, NGO_5
Known GenesIL12A-AS1, IQCJ-SCHIP1, SCHIP1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169610
Frequency
Sample Size93
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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