A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013296



Internal ID18755827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16909345..16932556hg38UCSC Ensembl
Innerchr1:17235840..17259051hg19UCSC Ensembl
Innerchr1:17108427..17131638hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3823212
hg1923212
hg1823212
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv123n100
Supporting Variantsnssv3474800
Samples
Known GenesCROCC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013296
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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