A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967931



Internal ID19233881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:93034901..93038001hg38UCSC Ensembl
OuterchrX:92289900..92293000hg19UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg383101
hg193101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113040
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967931
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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