A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046777



Internal ID19135996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34515619..34603622hg38UCSC Ensembl
Innerchr10:34804547..34892550hg19UCSC Ensembl
Innerchr10:34844553..34932556hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3888004
hg1988004
hg1888004
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707750
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)nsv1046777
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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