A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1086695



Internal ID15593195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:74194826..74282997hg38UCSC Ensembl
Innerchr7:73609156..73697327hg19UCSC Ensembl
Innerchr7:73247092..73335263hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3888172
hg1988172
hg1888172
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607481
Supporting Variants
Samples
Known GenesEIF4H, LAT2, RFC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1086695
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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