A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705113



Internal ID15095079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:64577976..64933558hg38UCSC Ensembl
Innerchr11:64345448..64701030hg19UCSC Ensembl
Innerchr11:64102024..64457606hg18UCSC Ensembl
Innerchr11:64102024..64457606hg17UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38355583
hg19355583
hg18355583
hg17355583
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528506
Supporting Variants
Samples
Known GenesATG2A, CDC42BPG, EHD1, MAP4K2, MEN1, MIR192, MIR194-2, MIR6749, MIR6750, NRXN2, PPP2R5B, PYGM, RASGRP2, SF1, SLC22A12
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705113
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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