A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1094499



Internal ID15600999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:128338766..128408140hg38UCSC Ensembl
Innerchr7:127978820..128048194hg19UCSC Ensembl
Innerchr7:127766056..127835430hg18UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3869375
hg1969375
hg1869375
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608400
Supporting Variants
Samples
Known GenesIMPDH1, PRRT4, RBM28
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1094499
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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