A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3469156



Internal ID19063222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:55965069..56003059hg38UCSC Ensembl
Innerchr1:56430742..56468732hg19UCSC Ensembl
Innerchr1:56203330..56241320hg18UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg3837991
hg1937991
hg1837991
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003385
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)nssv3469156
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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