A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018241



Internal ID18760774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88956339..88970626hg38UCSC Ensembl
Innerchr7:88585653..88599940hg19UCSC Ensembl
Innerchr7:88423589..88437876hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3814288
hg1914288
hg1814288
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655211
Samples
Known GenesZNF804B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018241
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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