A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013544



Internal ID18756075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16890896..16985316hg38UCSC Ensembl
Innerchr1:17217391..17311811hg19UCSC Ensembl
Innerchr1:17089978..17184398hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3894421
hg1994421
hg1894421
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv120n100
Supporting Variantsnssv3475578
Samples
Known GenesCROCC, MFAP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013544
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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