A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124472



Internal ID19258470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:121495396..121495462hg38UCSC Ensembl
Outerchr9:124257674..124257740hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959295, nssv3975764
SamplesKWS2, KWS1
Known GenesGGTA1P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124472
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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