A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608000



Internal ID16395409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:102461896..102469647hg38UCSC Ensembl
Innerchr7:102102343..102110094hg19UCSC Ensembl
Innerchr7:101889348..101897099hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg387752
hg197752
hg187752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11540n54
Supporting Variantsnssv1091994
Samples
Known GenesALKBH4, LRWD1, MIR5090
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608000
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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