A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999502



Internal ID19159039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:217353682..217411427hg38UCSC Ensembl
Innerchr1:217527024..217584769hg19UCSC Ensembl
Innerchr1:215593647..215651392hg18UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3857746
hg1957746
hg1857746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3500304
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)nsv999502
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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