A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3577283



Internal ID18528878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:68617209..68676278hg38UCSC Ensembl
Innerchr2:68844341..68903410hg19UCSC Ensembl
Innerchr2:68697845..68756914hg18UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg3859070
hg1959070
hg1859070
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003458
Supporting Variants
Samples
Known GenesPROKR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3577283
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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