A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597894



Internal ID16038617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:42628506..42630813hg38UCSC Ensembl
Innerchr5:42628608..42630915hg19UCSC Ensembl
Innerchr5:42664365..42666672hg18UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg382308
hg192308
hg182308
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9733n54
Supporting Variantsnssv1029155, nssv1029158, nssv1029154, nssv1029159, nssv1029160, nssv1029157, nssv1029156
Samples
Known GenesGHR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597894
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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