A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3964672



Internal ID19246408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:40645922..40646357hg38UCSC Ensembl
OuterchrX:40505174..40505609hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1111764
Supporting Variants
SamplesKWS2
Known GenesCXorf38
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3964672
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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