A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609209



Internal ID16049932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:156663585..156716626hg38UCSC Ensembl
Innerchr7:156456279..156509320hg19UCSC Ensembl
Innerchr7:156149040..156202081hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3853042
hg1953042
hg1853042
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1100519
Samples
Known GenesLMBR1, RNF32
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609209
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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