A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967928



Internal ID19239468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:40210947..40213147hg38UCSC Ensembl
OuterchrX:40070200..40072400hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg382201
hg192201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113038
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967928
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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