A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999872



Internal ID19159408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:37169903..37202094hg38UCSC Ensembl
Innerchr1:37635504..37667695hg19UCSC Ensembl
Innerchr1:37408091..37440282hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3832192
hg1932192
hg1832192
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3463095
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)nsv999872
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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