A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109957



Internal ID19263594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:58762652..58762912hg38UCSC Ensembl
OuterchrX:114670527..114670816hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38261
hg19290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4279n106
Supporting Variantsnssv3958405
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109957
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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