A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3581647



Internal ID18879928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:49020598..49202921hg38UCSC Ensembl
Innerchr2:49247737..49430060hg19UCSC Ensembl
Innerchr2:49101241..49283564hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38182324
hg19182324
hg18182324
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999566
Supporting Variants
Samples
Known GenesFSHR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3581647
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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