A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026853



Internal ID19116071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167934598..168192818hg38UCSC Ensembl
Innerchr6:168335278..168593498hg19UCSC Ensembl
Innerchr6:168078127..168336347hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38258221
hg19258221
hg18258221
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6199n100
Supporting Variantsnssv3655489, nssv3655479, nssv3749630, nssv3749629, nssv3655493, nssv3749634, nssv3749631, nssv3655481, nssv3655494, nssv3655495, nssv3655484, nssv3655491, nssv3749632, nssv3655487, nssv3655480, nssv3655492, nssv3655482, nssv3655485, nssv3655497, nssv3655488, nssv3749635, nssv3655496, nssv3749633, nssv3655490, nssv3655483, nssv3655486
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)nsv1026853
Frequency
Sample Size11257
Observed Gain26
Observed Loss0
Observed Complex0
Frequencyn/a


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