A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997975



Internal ID19157512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:177947133..178001835hg38UCSC Ensembl
Innerchr3:177664921..177719623hg19UCSC Ensembl
Innerchr3:179147615..179202317hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3854703
hg1954703
hg1854703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3614984
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997975
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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