A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3751509



Internal ID19049790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111528670..111726303hg38UCSC Ensembl
Innerchr7:111168726..111366359hg19UCSC Ensembl
Innerchr7:110955962..111153595hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38197634
hg19197634
hg18197634
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029531
Supporting Variants
Samples
Known GenesDOCK4, IMMP2L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3751509
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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