A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055841



Internal ID19145060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46130967..46286792hg38UCSC Ensembl
Innerchr17:44208333..44364158hg19UCSC Ensembl
Innerchr17:41564110..41719935hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38155826
hg19155826
hg18155826
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3195n100
Supporting Variantsnssv3720988, nssv3720987, nssv3720989
Samples
Known GenesKANSL1, KANSL1-AS1, LOC644172
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055841
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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