A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3988514



Internal ID18893365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1495591..1495708hg38UCSC Ensembl
Outerchr10:1537786..1537903hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1134974
Supporting Variants
SamplesKWS2
Known GenesADARB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3988514
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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