A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050176



Internal ID18792707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46467768..46861290hg38UCSC Ensembl
Innerchr10:46691159..47081683hg19UCSC Ensembl
Innerchr10:46111165..46501689hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38393523
hg19390525
hg18390525
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv742n100
Supporting Variantsnssv3519463
Samples
Known GenesBMS1P1, BMS1P5, FAM35BP, GLUD1P7, GPRIN2, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050176
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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