A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057914



Internal ID19147133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46136788..46286792hg38UCSC Ensembl
Innerchr17:44214154..44364158hg19UCSC Ensembl
Innerchr17:41569931..41719935hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38150005
hg19150005
hg18150005
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3195n100
Supporting Variantsnssv3550209, nssv3723909, nssv3550207, nssv3550205, nssv3550213, nssv3723910, nssv3723905, nssv3550204, nssv3723908, nssv3723906, nssv3723907, nssv3550210, nssv3550211, nssv3550212, nssv3550208, nssv3550206
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)nsv1057914
Frequency
Sample Size11257
Observed Gain11
Observed Loss5
Observed Complex0
Frequencyn/a


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