A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517553



Internal ID15444846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:42678701..42731284hg38UCSC Ensembl
Innerchr15:42970899..43023482hg19UCSC Ensembl
Innerchr15:40758191..40810774hg18UCSC Ensembl
Innerchr15:40758191..40810774hg17UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg3852584
hg1952584
hg1852584
hg1752584
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697941, nssv692747, nssv652340, nssv684349, nssv663669, nssv678472
Samples
Known GenesCDAN1, STARD9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517553
Frequency
Sample Size2026
Observed Gain1
Observed Loss5
Observed Complex0
Frequencyn/a


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