A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700467



Internal ID15090433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:45177416..45185503hg38UCSC Ensembl
Innerchr7:45217015..45225102hg19UCSC Ensembl
Innerchr7:45183540..45191627hg18UCSC Ensembl
Innerchr7:44990255..44998342hg17UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg388088
hg198088
hg188088
hg178088
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516731
Supporting Variants
Samples
Known GenesRAMP3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700467
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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