A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170174



Internal ID21314235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:128064298..128069358hg38UCSC Ensembl
Outerchr2:128060983..128069876hg38UCSC Ensembl
Innerchr2:128821872..128826932hg19UCSC Ensembl
Outerchr2:128818557..128827450hg19UCSC Ensembl
Innerchr2:128538342..128543402hg18UCSC Ensembl
Outerchr2:128535027..128543920hg18UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg388894
hg198894
hg188894
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14241494, nssv14243867, nssv14248216, nssv14250316
SamplesSNI_8, NGO_14, NGO_16, NGO_1
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170174
Frequency
Sample Size93
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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