A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143414



Internal ID18932331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:76353392..76365602hg38UCSC Ensembl
Outerchr7:75982709..75994919hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3812211
hg1912211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3980610
SamplesKWS1
Known GenesYWHAG
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143414
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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