A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14247657



Internal ID21305250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26392633..26397852hg38UCSC Ensembl
Outerchr3:26384700..26404482hg38UCSC Ensembl
Innerchr3:26434124..26439343hg19UCSC Ensembl
Outerchr3:26426191..26445973hg19UCSC Ensembl
Innerchr3:26409128..26414347hg18UCSC Ensembl
Outerchr3:26401195..26420977hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3819783
hg1919783
hg1819783
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169543
Supporting Variants
SamplesNGO_2
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14247657
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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