A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527202



Internal ID15454495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15999755..16000665hg38UCSC Ensembl
Innerchr4:16001378..16002288hg19UCSC Ensembl
Innerchr4:15610476..15611386hg18UCSC Ensembl
Innerchr4:15677647..15678557hg17UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38911
hg19911
hg18911
hg17911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703602
Samples
Known GenesPROM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527202
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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