A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176345



Internal ID15508330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:26734217..26789551hg38UCSC Ensembl
Innerchr13:27308354..27363688hg19UCSC Ensembl
Innerchr13:26206354..26261688hg18UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3855335
hg1955335
hg1855335
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561386
Supporting Variants
Samples1780862415_A
Known GenesGPR12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176345
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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