A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698975



Internal ID15435627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:87447271..87448680hg38UCSC Ensembl
Innerchr7:87076587..87077996hg19UCSC Ensembl
Innerchr7:86914523..86915932hg18UCSC Ensembl
Innerchr7:86721238..86722647hg17UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg381410
hg191410
hg181410
hg171410
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523246
Supporting Variants
Samples
Known GenesABCB4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698975
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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