A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997917



Internal ID19157453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:160587829..160878987hg38UCSC Ensembl
Innerchr2:161444340..161735498hg19UCSC Ensembl
Innerchr2:161152586..161443744hg18UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38291159
hg19291159
hg18291159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3582990
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)nsv997917
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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