A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169677



Internal ID21313488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:152982363..153000046hg38UCSC Ensembl
Outerchr1:152981901..153000835hg38UCSC Ensembl
Innerchr1:152954839..152972522hg19UCSC Ensembl
Outerchr1:152954377..152973311hg19UCSC Ensembl
Innerchr1:151221463..151239146hg18UCSC Ensembl
Outerchr1:151221001..151239935hg18UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3818935
hg1918935
hg1818935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14242205
SamplesNGO_36
Known GenesSPRR1A
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169677
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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