A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024819



Internal ID19114036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:27910336..27981350hg38UCSC Ensembl
Innerchr7:27949955..28020969hg19UCSC Ensembl
Innerchr7:27916480..27987494hg18UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg3871015
hg1971015
hg1871015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643327
Samples
Known GenesJAZF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024819
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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