A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005663



Internal ID19094880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:60200476..60472464hg38UCSC Ensembl
Innerchr4:61066194..61338182hg19UCSC Ensembl
Innerchr4:60748789..61020777hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38271989
hg19271989
hg18271989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3626517
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)nsv1005663
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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