A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3755295



Internal ID19053576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:69279160..69352409hg38UCSC Ensembl
Innerchr7:68744146..68817395hg19UCSC Ensembl
Innerchr7:68382082..68455331hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3873250
hg1973250
hg1873250
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028831
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3755295
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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