A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025546



Internal ID19114764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62589040..63299342hg38UCSC Ensembl
Innerchr7:62049418..62759720hg19UCSC Ensembl
Innerchr7:61686853..62397155hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38710303
hg19710303
hg18710303
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6411n100
Supporting Variantsnssv3661873
Samples
Known GenesZNF733P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025546
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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