A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3611353



Internal ID18909634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:192456837..192552148hg38UCSC Ensembl
Innerchr3:192174626..192269937hg19UCSC Ensembl
Innerchr3:193657320..193752631hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3895312
hg1995312
hg1895312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997731
Supporting Variants
Samples
Known GenesFGF12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3611353
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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