A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125929



Internal ID18926116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:152413611..152414219hg38UCSC Ensembl
Outerchr7:152110696..152111304hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3984132
SamplesKWS2
Known GenesKMT2C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125929
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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