A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14247585



Internal ID21301672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3862706..4058193hg38UCSC Ensembl
Outerchr3:3859793..4061917hg38UCSC Ensembl
Innerchr3:3904390..4099877hg19UCSC Ensembl
Outerchr3:3901477..4103601hg19UCSC Ensembl
Innerchr3:3879390..4074877hg18UCSC Ensembl
Outerchr3:3876477..4078601hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38202125
hg19202125
hg18202125
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169507
Supporting Variants
SamplesMLY_1
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14247585
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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