A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3474367



Internal ID19065944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:37167223..37221817hg38UCSC Ensembl
Innerchr1:37632824..37687418hg19UCSC Ensembl
Innerchr1:37405411..37460005hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3854595
hg1954595
hg1854595
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001914
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)nssv3474367
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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