A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032706



Internal ID18775240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167938968..168195239hg38UCSC Ensembl
Innerchr6:168339648..168595919hg19UCSC Ensembl
Innerchr6:168082497..168338768hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38256272
hg19256272
hg18256272
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6199n100
Supporting Variantsnssv3653048, nssv3653049
Samples
Known GenesFRMD1, HGC6.3, KIF25, KIF25-AS1, MLLT4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032706
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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