A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002929



Internal ID18745461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16855930..16927031hg38UCSC Ensembl
Innerchr1:17182425..17253526hg19UCSC Ensembl
Innerchr1:17055012..17126113hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3871102
hg1971102
hg1871102
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv105n100
Supporting Variantsnssv3466966, nssv3700141
Samples
Known GenesCROCC, MIR3675
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002929
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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