A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007222



Internal ID19096441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:56662277..56678853hg38UCSC Ensembl
Innerchr4:57528443..57545019hg19UCSC Ensembl
Innerchr4:57223200..57239776hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3816577
hg1916577
hg1816577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3625291
Samples
Known GenesHOPX
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007222
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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