A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997637



Internal ID19157174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:46424485..46449489hg38UCSC Ensembl
Innerchr2:46651624..46676628hg19UCSC Ensembl
Innerchr2:46505128..46530132hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3825005
hg1925005
hg1825005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3805n100
Supporting Variantsnssv3581627, nssv3581626
Samples
Known GenesLOC101805491
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997637
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer