A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027893



Internal ID19117111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62720720..63332411hg38UCSC Ensembl
Innerchr7:62181098..62792789hg19UCSC Ensembl
Innerchr7:61818533..62430224hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38611692
hg19611692
hg18611692
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6429n100
Supporting Variantsnssv3661949
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)nsv1027893
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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