A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662029



Internal ID18960310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:112452654..112500375hg38UCSC Ensembl
Innerchr7:112092709..112140430hg19UCSC Ensembl
Innerchr7:111879945..111927666hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3847722
hg1947722
hg1847722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030033
Supporting Variants
Samples
Known GenesIFRD1, LSMEM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3662029
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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