A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025619



Internal ID18768151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89018127..89047196hg38UCSC Ensembl
Innerchr7:88647441..88676510hg19UCSC Ensembl
Innerchr7:88485377..88514446hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3829070
hg1929070
hg1829070
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6527n100
Supporting Variantsnssv3655214
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)nsv1025619
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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