A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14251095



Internal ID21306353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:78324847..79014630hg38UCSC Ensembl
Outerchr2:78319793..79014684hg38UCSC Ensembl
Innerchr2:78551973..79241756hg19UCSC Ensembl
Outerchr2:78546919..79241810hg19UCSC Ensembl
Innerchr2:78405481..79095264hg18UCSC Ensembl
Outerchr2:78400427..79095318hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38694892
hg19694892
hg18694892
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169744
Supporting Variants
SamplesNGO_27
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14251095
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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