A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984501



Internal ID19208169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:111430642..111431242hg38UCSC Ensembl
Outerchr10:113190400..113191000hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126268
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984501
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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