A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1079770



Internal ID15932956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:22162867..22196207hg38UCSC Ensembl
Innerchr7:22202485..22235825hg19UCSC Ensembl
Innerchr7:22169010..22202350hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3833341
hg1933341
hg1833341
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606405
Supporting Variants
Samples
Known GenesRAPGEF5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1079770
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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