A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524157



Internal ID15104764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:155054466..155058081hg38UCSC Ensembl
Innerchr1:155026942..155030557hg19UCSC Ensembl
Innerchr1:153293566..153297181hg18UCSC Ensembl
Innerchr1:151840015..151843630hg17UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg383616
hg193616
hg183616
hg173616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700036
Samples
Known GenesADAM15, LOC100505666
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524157
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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