A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010002



Internal ID19099221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:12772..75345hg38UCSC Ensembl
Innerchr2:12772..75345hg19UCSC Ensembl
Innerchr2:2772..65345hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3862574
hg1962574
hg1862574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3570481
Samples
Known GenesFAM110C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010002
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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