A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580807



Internal ID18879088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:130001889..130067873hg38UCSC Ensembl
Innerchr2:130759462..130825446hg19UCSC Ensembl
Innerchr2:130475932..130541916hg18UCSC Ensembl
Cytoband2q21.1
Allele length
AssemblyAllele length
hg3865985
hg1965985
hg1865985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010484
Supporting Variants
Samples
Known GenesFAR2P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3580807
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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