A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047925



Internal ID18790456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:97603..270899hg38UCSC Ensembl
Innerchr10:143543..316839hg19UCSC Ensembl
Innerchr10:133543..306839hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38173297
hg19173297
hg18173297
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv650n100
Supporting Variantsnssv3496393
Samples
Known GenesZMYND11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047925
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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