A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966932



Internal ID19245605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:95519463..95519731hg38UCSC Ensembl
OuterchrX:45587559..45587866hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38269
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1130618
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966932
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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