A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065586



Internal ID19154805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46185584..46286792hg38UCSC Ensembl
Innerchr17:44262950..44364158hg19UCSC Ensembl
Innerchr17:41618727..41719935hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38101209
hg19101209
hg18101209
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3234n100
Supporting Variantsnssv3725332, nssv3557342, nssv3557338, nssv3725330, nssv3725336, nssv3725331, nssv3725335, nssv3725334, nssv3557339, nssv3725337, nssv3724221, nssv3557341, nssv3725333, nssv3725329, nssv3557343, nssv3557337, nssv3557340, nssv3557336
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)nsv1065586
Frequency
Sample Size11257
Observed Gain8
Observed Loss10
Observed Complex0
Frequencyn/a


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