A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057856



Internal ID19147075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:27643961..27749600hg38UCSC Ensembl
Innerchr17:25970987..26076626hg19UCSC Ensembl
Innerchr17:22995114..23100753hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg38105640
hg19105640
hg18105640
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3137n100
Supporting Variantsnssv3561038, nssv3561039
Samples
Known GenesLGALS9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057856
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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