A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14250769



Internal ID21309930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:132273929..132276840hg38UCSC Ensembl
Outerchr3:132273893..132281633hg38UCSC Ensembl
Innerchr3:131992773..131995684hg19UCSC Ensembl
Outerchr3:131992737..132000477hg19UCSC Ensembl
Innerchr3:133475463..133478374hg18UCSC Ensembl
Outerchr3:133475427..133483167hg18UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg387741
hg197741
hg187741
Variant TypeCNV deletion
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169742
Supporting Variants
SamplesNGO_53
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14250769
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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