A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018486



Internal ID19107703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65190920..65641881hg38UCSC Ensembl
Innerchr7:64651298..65106792hg19UCSC Ensembl
Innerchr7:64288733..64744227hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38450962
hg19455495
hg18455495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6435n100
Supporting Variantsnssv3655562, nssv3655564, nssv3655560, nssv3655561, nssv3655565, nssv3655563
Samples
Known GenesZNF92
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018486
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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