A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3494051



Internal ID19081692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:104562716..104633369hg38UCSC Ensembl
Innerchr1:105105338..105175991hg19UCSC Ensembl
Innerchr1:104906861..104977514hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3870654
hg1970654
hg1870654
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013052
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)nssv3494051
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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