A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729314



Internal ID19027595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:194043206..194112012hg38UCSC Ensembl
Innerchr2:194907930..194976736hg19UCSC Ensembl
Innerchr2:194616175..194684981hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3868807
hg1968807
hg1868807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013191
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3729314
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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