A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174504



Internal ID15507127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46216824..46279254hg38UCSC Ensembl
Innerchr10:47588060..47650490hg19UCSC Ensembl
Innerchr10:47058066..47120496hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3862431
hg1962431
hg1862431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550770
Supporting Variants
Samples1780854449_A
Known GenesANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174504
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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