A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3974213



Internal ID18882679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:10905429..10905485hg38UCSC Ensembl
Outerchr6:10905662..10905718hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1124031
Supporting Variants
SamplesKWS2
Known GenesSYCP2L
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3974213
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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