A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3478126



Internal ID19067922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:34622883..34638878hg38UCSC Ensembl
Innerchr1:35088484..35104479hg19UCSC Ensembl
Innerchr1:34861071..34877066hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3815996
hg1915996
hg1815996
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008561
Supporting Variants
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)nssv3478126
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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