A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3982375



Internal ID18857349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:21940782..21941482hg38UCSC Ensembl
OuterchrX:21958900..21959600hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145287
Supporting Variants
SamplesKWS1
Known GenesSMS
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3982375
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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