A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035250



Internal ID18777781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46416662..46481242hg38UCSC Ensembl
Innerchr10:47068215..47133089hg19UCSC Ensembl
Innerchr10:46488221..46553095hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3864581
hg1964875
hg1864875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv813n100
Supporting Variantsnssv3705907
Samples
Known GenesLINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035250
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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