A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998767



Internal ID18811617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16909345..16931137hg38UCSC Ensembl
Innerchr1:17235840..17257632hg19UCSC Ensembl
Innerchr1:17108427..17130219hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3821793
hg1921793
hg1821793
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv123n100
Supporting Variantsnssv3479392
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)nsv998767
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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