A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010078



Internal ID19099297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:19077756..19384899hg38UCSC Ensembl
Innerchr4:19079379..19386522hg19UCSC Ensembl
Innerchr4:18688477..18995620hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38307144
hg19307144
hg18307144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3737706
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)nsv1010078
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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