A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960424



Internal ID19213526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:3483795..3483922hg38UCSC Ensembl
OuterchrX:3401836..3401963hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128528
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960424
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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