A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007436



Internal ID19096655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:82663550..82711909hg38UCSC Ensembl
Innerchr1:83129233..83177592hg19UCSC Ensembl
Innerchr1:82901821..82950180hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3848360
hg1948360
hg1848360
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3699595
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)nsv1007436
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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