A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3707751



Internal ID19006032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34618606..34677063hg38UCSC Ensembl
Innerchr10:34907534..34965991hg19UCSC Ensembl
Innerchr10:34947540..35005997hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3858458
hg1958458
hg1858458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050107
Supporting Variants
Samples
Known GenesPARD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3707751
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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