A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3579793



Internal ID18878074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89896137..90079966hg38UCSC Ensembl
Innerchr2:89934947..90118808hg19UCSC Ensembl
Innerchr2:89571989..89756113hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38183830
hg19183862
hg18184125
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011639
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)nssv3579793
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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