A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035634



Internal ID18778165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73724401..73907300hg38UCSC Ensembl
Innerchr10:75484159..75667058hg19UCSC Ensembl
Innerchr10:75154165..75337064hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38182900
hg19182900
hg18182900
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503975
Samples
Known GenesBMS1P4, CAMK2G, CHCHD1, FUT11, GLUD1P3, NDST2, SEC24C, ZSWIM8, ZSWIM8-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035634
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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