A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005574



Internal ID19094791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:91448064..91458377hg38UCSC Ensembl
Innerchr1:91913621..91923934hg19UCSC Ensembl
Innerchr1:91686209..91696522hg18UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3810314
hg1910314
hg1810314
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3473795
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)nsv1005574
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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