A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3752783



Internal ID18704378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:181005..231133hg38UCSC Ensembl
Innerchr7:181005..231133hg19UCSC Ensembl
Innerchr7:276088..326216hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3850129
hg1950129
hg1850129
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026359
Supporting Variants
Samples
Known GenesFAM20C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3752783
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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