A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607931



Internal ID16048654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:100067194..100198523hg38UCSC Ensembl
Innerchr7:99664817..99796146hg19UCSC Ensembl
Innerchr7:99502753..99634082hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38131330
hg19131330
hg18131330
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1091650
Samples
Known GenesAP4M1, C7orf43, CNPY4, COPS6, GAL3ST4, GPC2, LAMTOR4, MBLAC1, MCM7, MIR106B, MIR25, MIR4658, MIR93, STAG3, TAF6, ZNF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607931
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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