A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3553614



Internal ID18505209
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 StatusS
Merged Variantsnsv1035640
Supporting Variants
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)nssv3553614
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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