A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006603



Internal ID19095820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:57382200..57485359hg38UCSC Ensembl
Innerchr2:57609335..57712494hg19UCSC Ensembl
Innerchr2:57462839..57565998hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38103160
hg19103160
hg18103160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3577231
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)nsv1006603
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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