A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035640



Internal ID18778171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58813161..58898731hg38UCSC Ensembl
Innerchr15:59105360..59190930hg19UCSC Ensembl
Innerchr15:56892652..56978222hg18UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg3885571
hg1985571
hg1885571
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553614
Samples
Known GenesFAM63B, SLTM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035640
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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