A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997911



Internal ID19157447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:62333197..62374919hg38UCSC Ensembl
Innerchr2:62560332..62602054hg19UCSC Ensembl
Innerchr2:62413836..62455558hg18UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3841723
hg1941723
hg1841723
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3730853
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)nsv997911
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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