A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007037



Internal ID18749568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:157572438..157675815hg38UCSC Ensembl
Innerchr2:158428950..158532327hg19UCSC Ensembl
Innerchr2:158137196..158240573hg18UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38103378
hg19103378
hg18103378
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3729266
Samples
Known GenesACVR1C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007037
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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