A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126268



Internal ID19279337
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 StatusM
Merged Variantsdgv515n106
Supporting Variantsnssv3984501
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126268
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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