A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030063



Internal ID19119282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2691667..2729595hg38UCSC Ensembl
Innerchr9:2691667..2729595hg19UCSC Ensembl
Innerchr9:2681667..2719595hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3837929
hg1937929
hg1837929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3692364
Samples
Known GenesKCNV2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030063
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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