A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519576



Internal ID18817857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45525733..45592613hg38UCSC Ensembl
Innerchr10:46021181..46088061hg19UCSC Ensembl
Innerchr10:45341187..45408067hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3866881
hg1966881
hg1866881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041417
Supporting Variants
Samples
Known GenesMARCH8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3519576
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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