A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121528



Internal ID18909726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:76706317..76706376hg38UCSC Ensembl
Outerchr17:74702399..74702458hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3965531
SamplesKWS2
Known GenesMXRA7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121528
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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