A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005415



Internal ID19094632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:5742013..5760597hg38UCSC Ensembl
Innerchr1:5802073..5820657hg19UCSC Ensembl
Innerchr1:5724660..5743244hg18UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3818585
hg1918585
hg1818585
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3473594
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)nsv1005415
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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