A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025214



Internal ID18767746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89018127..89040085hg38UCSC Ensembl
Innerchr7:88647441..88669399hg19UCSC Ensembl
Innerchr7:88485377..88507335hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3821959
hg1921959
hg1821959
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6527n100
Supporting Variantsnssv3655213
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)nsv1025214
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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