A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018445



Internal ID18760978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62589040..64779945hg38UCSC Ensembl
Innerchr7:62049418..64240323hg19UCSC Ensembl
Innerchr7:61686853..63877758hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg382190906
hg192190906
hg182190906
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3753025
Samples
Known GenesLINC01005, LOC100128885, LOC100287704, LOC100287834, LOC641746, MIR4283-1, MIR4283-2, MIR6839, YWHAEP1, ZNF107, ZNF679, ZNF680, ZNF727, ZNF733P, ZNF735, ZNF736
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018445
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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