A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661214



Internal ID18612809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40449484..40503334hg38UCSC Ensembl
Innerchr7:40489083..40542933hg19UCSC Ensembl
Innerchr7:40455608..40509458hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3853851
hg1953851
hg1853851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029342
Supporting Variants
Samples
Known GenesC7orf10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3661214
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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