A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665572



Internal ID15055538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:125388505..125460745hg38UCSC Ensembl
Innerchr9:128150784..128223024hg19UCSC Ensembl
Innerchr9:127190605..127262845hg18UCSC Ensembl
Innerchr9:125230338..125302578hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3872241
hg1972241
hg1872241
hg1772241
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515979
Supporting Variants
Samples
Known GenesMAPKAP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665572
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer