A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006995



Internal ID19096213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:163764124..163918955hg38UCSC Ensembl
Innerchr1:163733361..163888192hg19UCSC Ensembl
Innerchr1:161999985..162154816hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38154832
hg19154832
hg18154832
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv457n100
Supporting Variantsnssv3491468
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)nsv1006995
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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