A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173636



Internal ID15532342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46331279hg38UCSC Ensembl
Innerchr10:47543322..47702515hg19UCSC Ensembl
Innerchr10:47013328..47172521hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38159194
hg19159194
hg18159194
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550754
Supporting Variants
SamplesHGDP01296
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173636
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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