A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016602



Internal ID19105821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:63163053..63879429hg38UCSC Ensembl
Innerchr7:62623431..63339807hg19UCSC Ensembl
Innerchr7:62260866..62977242hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38716377
hg19716377
hg18716377
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3661963
Samples
Known GenesLOC100287704, LOC100287834, MIR4283-1, MIR4283-2, ZNF733P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016602
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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